BD 4 Fr Single-Lumen PowerPICC Catheters, REF: 3174155… recallZ-1507-2025 · Bard Access Systems, Inc. · initiated Mar 11, 2025
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Bard Access Systems, Inc. or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Catheters indicated for short-or-long term access to the central venous system have tubing that exceeded melt flow index specification (higher), which could lead to increased material fatigue leaks, which could lead to infiltration, extravasation, discomfort, phlebitis, bleeding, air embolism, foreign body embolism, infection and interruption to therapy.
FDA root cause category: Process control
What the company is doing
On 3/11/2025, recall notices were distributed to customers and distributors who were asked to do the following: Actions if catheter damage is suspected: 1. Stop any infusion if catheter damage is suspected. 2. Follow your institution's guidelines for catheters with suspected damage. 3. If catheter fracture is confirmed, catheter should be removed and an alternative route for access should be obtained. 4. Report any catheter replacements due to leakage to firm's Complaint Center. Please Take the Following Actions: 1. Destroy all unused product following your institution's process for destruction. 2. If affected device was previously used on a patient without incident, no further action is necessary. 3. Recall notice should be shared with anyone who needs to be aware within your organization and forwarded to any organization where potentially affected devices have been transferred. 4. Complete and return Customer Response Form via email to Email: [email protected] Distributors asked to identify all customers within distribution network that purchased any affected product. Provide a copy of the attached customer letter to all customers to advise them of this recall Actions Taken by Firm: 2. Firm is notifying users that adhesive-backed securement systems are recommended. 3. Firm is notifying users that if they do use compression-style securement systems, they must be sized appropriately to accommodate the taper region. 4. Firm has been updating the product IFU with cautions related to the use of compression-style securement systems around the taper region of the PICC. 5. Firm is notifying customers to insert the catheter as close as possible to the zero mark per the IFU. For further assistance, contact: North American Regional Complaint Center: 1-844-823-5433 Mon-Fri 8:00am and 5:00pm CT or [email protected]. On 5/15/2025 additional recall notices were distributed to customers informing them of additional affected devices.
Recall details
- Recall number
- Z-1507-2025
- Status
- Open, Classified
- Initiated by the company
- Mar 11, 2025
- Posted by the FDA
- Apr 16, 2025
- Recalling firm
- Bard Access Systems, Inc.
- Quantity
- 718,461
- Product code
- LJS
- FDA submissions
- K210264
- Distribution
- Worldwide - US Nationwide distribution including in the states of WI, NC, TX, NY, CA, MN, MT, RI, MA, OH, CT, SC, IL, CO, VA, NJ, GA, UT, FL, PA, IN, MD, KY, AZ, MI, WA, HI, MO, VT, AL, NM, TN, DE, LA, IA, NH, ID, DC, WV, KS, NE, SD, ND, WY, AK, OK, OR, AR and the countries of Andorra, Australia, Austria, Belgium, Brazil, Canada, Chile, China, Colombia, Costa Rica, Czech Republic, Denmark, Finland, France, French Polynesia, French Guayana, Germany, Greece, Guadeloupe, Guatemala, Hong Kong, Hungary, India, Ireland, Israel, Italy, Japan, Jordan, Kuwait, Luxembourg, Martinique, Mexico, Netherlands, New Caledonia, New Zealand, Norway, Pakistan, Poland, Portugal, Qatar, Republic of Korea, Reunion, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan, Turkey, United Arab Emirates, United Kingdom, Viet Nam.
Product description
BD 4 Fr Single-Lumen PowerPICC Catheters, REF: 3174155, CK000540, 3174118, CK000483, 3174335, 3174355, CK000196, 9174118, CK000955, 3174135, CK000617, CK000839, 3194355, 6174118, 3194135, 3194335, 2174108, 9194118, 3194118, 1174118, CK000285C, CK000335A, CK000796, 1194108D, CK000757, CK001042, 9174108, 1174108D1, CK000631B, 3194155, 3174108, CK000567, 1194108D4, 1174108D2, CK000677, CK000864, CK000937A, CK000930, CK001027, 1174108D, CK000867, CK000900, CK000315A, CK000589A, CK000854B, CK000897, CK000953A, CK000586B, CK000549, CK000844, 1194108D1, 1174108D4, 1194108D3, CK000934, CK000986, CK000411, CK001018, 1174108, CK000060, CK000513A, CK001021, CK001030, CK000501A, CK000619A, CK000903, 3194108, 1194108D2, 9194108D, CK000959, CK000613, CK000991, CK000983, CK000881, CK000721, CK000642, CK000289C, CK000894A, CK000914, CK000445, CK000687, CK000524A, CK000819, CK000266A, 1174108D3, 3194108D, CK000545, 1174108D5, 3174108D, CK000775A, 1194108D5, CK000736, CK000739, 9194108, 1194108, CK000660, CK000609A, 9174108D, CK001067, CK000077D, CK000882, CK000874, CK000994, CK000870A, CK000443C, CK000668B, CK000784
Code information (models, lots, serial numbers)
Show the full code information (12k characters)
REF/UDI-DI/Lot(Expiration): 3174155/00801741027611/REGQ0844(6/30/2025), REGZ1439(11/30/2025), REHP0860(11/30/2025), REHQ3097(6/30/2026), REHR0022(6/30/2026), REHT1151(7/31/2026), REHU1525(11/30/2026), REHU2455(6/30/2026), REHU2614(11/30/2026), REHV2765 (7/31/2026), REJN3472(2/28/2027), REJP4216(5/31/2027), REJQ2272(7/31/2027), REJR1411(8/31/2027), REJR2565(4/30/2027), REJR2614(8/31/2027), REJT0755(9/30/2027); CK000540/00801741105142/REGZ1425(10/31/2025), REHP0808(11/30/2025), REHU1513(1/31/2026), REHV2221(1/31/2026), REHY2842(10/31/2026), REJN4145 (12/31/2026), REJR1322(3/31/2027), REJS2110(4/30/2027), REJS3773(2/28/2027); 3174118/00801741027598/REGZ2512(11/30/2025), REHP1760(1/31/2026), REHP2603(1/31/2026), REJN1059(12/31/2026); CK000483/00801741099397/REHN3187(10/31/2025), REHQ1804(6/30/2026), REJN1065(5/31/2027), REJP2018(6/30/2027), REJR1321(8/31/2027); 3174335/00801741027628/REHN3908(10/31/2025), REHP0800(10/31/2025), REHQ3070(11/30/2025), REHT1129(5/31/2026), REHU1519(6/30/2026), REHV1391(7/31/2026), REHV3050(7/31/2026), REHZ1011(11/30/2026), REJN4109(12/31/2026), REJQ0405(2/28/2027), REJR2090(3/31/2027), REJT0833(5/31/2027); 3174355/00801741027635/REHQ1781(11/30/2025), REHS1925(4/30/2026), REHT1120(5/31/2026), REHU0975(6/30/2026), REHU2488(6/30/2026), REHV1400(7/31/2026), REHV3020(7/31/2026), REHW1329(8/31/2026), REHY1684(10/31/2026), REHZ1903(11/30/2026), REJN3007(12/31/2026), REJP0855(1/31/2027), REJP2021(1/31/2027), REJQ2284(2/28/2027), REJR2157(3/31/2027), REJS2171(4/30/2027), REJS4490(4/30/2027); CK000196/00801741028847/REHQ3064(6/30/2026), REHT2954(1/31/2026), REHX2926(12/31/2026), REHZ1873(3/31/2027), REJQ2279(8/31/2027); 9174118/00801741035562/REHQ3091(6/30/2026), REHR0017(6/30/2026), REHT1132(6/30/2026), REHU2496(6/30/2026), REHY2811(2/28/2026), REHZ1882(3/31/2027); CK000955/00801741200922/REHQ4029(11/30/2025), REHV2232(2/28/2026), REHX2916(12/31/2025), REHY3954(7/31/2026), REJN2995(9/30/2025); 3174135/00801741027604/REHR0003(11/30/2025), REHS4184(7/31/2026), REHU2356(11/30/2026), REHU2612(6/30/2026), REJS2089(9/30/2027); CK000617/00801741122286/REHS1001(9/30/2025), REJQ2280(2/28/2027); CK000839/00801741154393/REHS4241(4/30/2026), REHV3026(7/31/2026), REHX2908(9/30/2026), REHY2826(10/31/2026), REJN3000(12/31/2026), REJS3479(4/30/2027); 3194355/00801741027789/REHT2157(5/31/2025), REHT2967(5/31/2025), REHU3317(6/30/2025), REHV3031(7/31/2025), REHY3957(10/31/2025), REHZ1878(11/30/2025), REJN3008(12/31/2025), REJR1276(12/31/2025), REJR2062(3/31/2026), REJS2065(12/31/2025); 6174118/00801741139017/REHT2984(1/31/2026); 3194135/00801741027758/REHU1029(5/31/2025), REHY1636(10/31/2025), REHY2820(10/31/2025), REJN2980(12/31/2025); 3194335/00801741027772/REHU1430(6/30/2025), REHU2339(6/30/2025), REHW1354(8/31/2025), REHY2700(10/31/2025), REHZ1026(10/31/2025), REJN1463(12/31/2025), REJN3016(12/31/2025), REJR2013(3/31/2026), REJS3853(12/31/2025); 2174108/00801741138966/REHU3327(9/30/2025); 9194118/00801741028618/REHV0263(6/30/2025), REJQ0411(1/31/2026); 3194118/00801741027741REHY1654(10/31/2025), REJP0843(5/31/2025), REJS0206(3/31/2026); 1174118/00801741034466/REHY2815(5/31/2025), REJN1443(8/31/2025), REJQ0415(5/31/2025), REJQ2243(8/31/2025), REJS4488(10/31/2025); CK000285C/00801741161117/REHZ1477(5/31/2025), REJN2365(5/31/2025), REJQ2812(8/31/2025), REJR2208(9/30/2025), REJS1287(9/30/2025), REJS4740(10/31/2025); CK000335A/00801741101281/REHZ1620(5/31/2025), REJN2425(6/30/2025), REJQ0819(8/31/2025), REJQ1491(8/31/2025); CK000796/00801741144783/REHZ1625(5/31/2025), REJQ1521(8/31/2025), REJR1458(9/30/2025), REJS0258(9/30/2025), REJS3583(10/31/2025), REJT0877(11/30/2025), REJX0310(2/28/2026); 1194108D/00801741034510/REHZ1633(5/31/2025), REJN3882(5/31/2025), REJN3972(6/30/2025), REJP4057(7/31/2025), REJP4060(7/31/2025), REJP4066(7/31/2025), REJP4068(7/31/2025), REJR2209(9/30/2025), REJR2227(9/30/2025), REJS1269(9/30/2025), REJS2211(9/30/2025), REJS3526(10/31/2025), REJU1142(10/31/2025), REJV3948(1/31/2026); CK000757/00801741141133/REHZ1652(5/31/2025), REJQ0793(6/30/2025), REJR1443(8/31/2025), REJS1253(7/31/2025), REJS3543(8/31/2025), REJV0288(10/31/2025); CK001042/00801741224324/REHZ1657(5/31/2025), REJN2389(6/30/2025), REJR1448(9/30/2025), REJT0890(11/30/2025); 9174108/00801741035548/REJN0035(6/30/2025), REJQ0431(8/31/2025), REJR0582(9/30/2025); 1174108D1/00801741154737/REJN0722(5/31/2025), REJP1731(7/31/2025), REJR0469(8/31/2025), REJR2556(9/30/2025), REJS2083(10/31/2025); CK000631B/00801741143748/REJN0748(5/31/2025), REJP2723(7/31/2025), REJP2747(7/31/2025), REJS1310(9/30/2025), REJS4709(10/31/2025); 3194155/00801741027765/REJN0964(6/30/2025), REJN1080(6/30/2025), REJN4126(6/30/2025), REJQ0418(8/31/2025), REJS3757(10/31/2025), REJT1225(11/30/2025); 3174108/00801741027574/REJN1098(6/30/2025), REJR2206(9/30/2025), REJS2212(10/31/2025); CK000567/00801741108167/REJN1450(5/31/2025), REJQ0400(8/31/2025); 1194108D4/00801741155093/REJN2245(5/31/2025), REJP1828(7/31/2025), REJQ1321(6/30/2025), REJR0440(6/30/2025), REJR2590(7/31/2025), REJS2165(7/31/2025), REJS4634(7/31/2025); 1174108D2/00801741154836/REJN2302(5/31/2025), REJP1701(5/31/2025), REJQ1440(8/31/2025), REJR1289(9/30/2025), REJR2589(9/30/2025), REJS2453(10/31/2025), REJS4511(9/30/2025), REJU1046(11/30/2025); CK000677/00801741131790/REJN2329(5/31/2025), REJR1433(9/30/2025), REJS3919(10/31/2025); CK000864/00801741163302/REJN2340(5/31/2025), REJR1423(7/31/2025), REJR2685(7/31/2025), REJS2226(6/30/2025); CK000937A/00801741224003/REJN2347(5/31/2025), REJQ0824(6/30/2025), REJR2631(7/31/2025), REJS3571(8/31/2025); CK000930/00801741188091/REJN2351(5/31/2025), REJR2649(9/30/2025); CK001027/00801741223921/REJN2359(5/31/2025), REJR2690(9/30/2025), REJT1434(9/30/2025); 1174108D/00801741034459/REJN2362(5/31/2025), REJN2363(5/31/2025), REJP4065(7/31/2025), REJQ0816(8/31/2025), REJR0595(9/30/2025), REJR0600(9/30/2025), REJR2677(9/30/2025), REJS1284(9/30/2025), REJS2210(10/31/2025), REJS3915(10/31/2025), REJS4729(10/31/2025); CK000867/00801741163272/REJN2377(5/31/2025); CK000900/00801741184956/REJN2381(5/31/2025), REJR0589(6/30/2025), REJR1461(6/30/2025), REJS1259(6/30/2025), REJS2603(6/30/2025); CK000315A/00801741182723/REJN2391(6/30/2025), REJN3978(5/31/2025), REJQ2835(8/31/2025), REJR2697(9/30/2025), REJT1407(11/30/2025); CK000589A/00801741137624/REJN2395(6/30/2025), REJR2198(7/31/2025); CK000854B/00801741225802/REJN2400(6/30/2025), REJN3856(6/30/2025), REJQ2816(8/31/2025), REJS1317(9/30/2025), REJT0876(11/30/2025); CK000897/00801741184925/REJN2404(6/30/2025), REJN3860(6/30/2025), REJQ2807(6/30/2025), REJR2686(7/31/2025), REJS0277(7/31/2025), REJS1295(6/30/2025), REJT0874(7/31/2025); CK000953A/00801741223303/REJN2409(6/30/2025), REJS2228(8/31/2025), REJV1726(1/31/2026); CK000586B/00801741212789/REJN2420(6/30/2025), REJR1455(6/30/2025), REJR2211(7/31/2025); CK000549/00801741107313/REJN2427(6/30/2025), REJU2672(12/31/2025); CK000844/00801741154690/REJN3737(5/31/2025), REJS0060(9/30/2025); 1194108D1/00801741154782/REJN3778(5/31/2025), REJQ1238(8/31/2025), REJR2004(8/31/2025), REJS1173(7/31/2025); 1174108D4/00801741155048/REJN3820(5/31/2025), REJP1880(7/31/2025), REJR0536(6/30/2025), REJR1407(8/31/2025), REJR2563(6/30/2025), REJS2541(8/31/2025), REJS3729(7/31/2025); 1194108D3/00801741154997/REJN3821(5/31/2025), REJP3949(5/31/2025), REJR0537(9/30/2025), REJR2557(7/31/2025), REJS2084(10/31/2025), REJS4512(10/31/2025), REJU0239(11/30/2025); CK000934/00801741188381/REJN3864(6/30/2025), REJQ1483(8/31/2025), REJS4722(10/31/2025); CK000986/00801741216008/REJN3867(6/30/2025), REJN3923(5/31/2025), REJQ0825(7/31/2025), REJQ1499(7/31/2025), REJR2670(9/30/2025), REJS1324(10/31/2025), REJS4724(10/31/2025); CK000411/00801741096303/REJN3872(5/31/2025); CK001018/00801741222993/REJN3880(6/30/2025), REJQ1526(8/31/2025), REJT1397(9/30/2025); 1174108/00801741034442/REJN3881(5/31/2025), REJQ0432(8/31/2025), REJR2638(9/30/2025); CK000060/00801741028731/REJN3891(6/30/2025), REJQ0799(8/31/2025), REJQ1517(8/31/2025), REJR1432(9/30/2025), REJS1329(10/31/2025), REJS3916(10/31/2025); CK000513A/00801741110030/REJN3898(5/31/2025), REJS3539(8/31/2025); CK001021/00801741222863/REJN3927(6/30/2025) CK001030/00801741223976/REJN3970(6/30/2025), REJS0262(8/31/2025); CK000501A/00801741140815/REJN3980(6/30/2025), REJR2220(9/30/2025), REJT1408(11/30/2025), REJU2651(12/31/2025); CK000619A/00801741132001/REJN3985(6/30/2025); CK000903/00801741183089/REJN3999(6/30/2025), REJS0283(9/30/2025), REJT0909(11/30/2025); 3194108/00801741027710/REJN4166(6/30/2025), REJS3535(10/31/2025); 1194108D2/00801741154881/REJP0630(7/31/2025), REJR0470(8/31/2025), REJR0502(9/30/2025), REJS2556(10/31/2025); 9194108D/00801741035609/REJP1767(7/31/2025), REJR2695(9/30/2025); CK000959/00801741200960/REJP1942(7/31/2025), REJQ1524(8/31/2025), REJS0284(9/30/2025); CK000613/00801741121395/REJP1943(7/31/2025), REJQ1493(8/31/2025), REJR1670(9/30/2025), REJS0293(9/30/2025), REJS2216(10/31/2025), REJS4779(10/31/2025), REJV1721(1/31/2026); CK000991/00801741213298/REJP1950(5/31/2025), REJQ1512(8/31/2025), REJT1415(9/30/2025); CK000983/00801741225734/REJP2027(7/31/2025), REJP4183(7/31/2025), REJS1105(10/31/2025), REJS3409(10/31/2025); CK000881/00801741188787/REJP2717(7/31/2025), REJR1424(8/31/2025); CK000721/00801741137655/REJP2725(7/31/2025), REJR2213(9/30/2025), REJS1291(9/30/2025), REJT1365(11/30/2025); CK000642/00801741127908/REJP2727(7/31/2025), REJT0895(10/31/2025); CK000289C/00801741161148/REJP2728(7/31/2025), REJQ0813(8/31/2025), REJR2219(9/30/2025), REJS2203(9/30/2025), REJT1406(11/30/2025), REJV0222(9/30/2025), REJV1719(9/30/2025), REJX3527(1/31/2026); CK000894A/00801741188732/REJP2737(5/31/2025), REJS2218(10/31/2025); CK000914/00801741202599/REJP2741(7/31/2025), REJR1425(8/31/2025), REJS1319(9/30/2025), REJT0899(11/30/2025); CK000445/00801741101557/REJP2744(7/31/2025), REJR2662(9/30/2025); CK000687/00801741136535/REJP2746(6/30/2025), REJV3817(9/30/2025); CK000524A/00801741124068/REJP2748(6/30/2025), REJR1418(7/31/2025); CK000819/00801741152566/REJP2750(6/30/2025), REJS0294(6/30/2025); CK000266A/00801741185014/REJP2755(7/31/2025); 1174108D3/00801741154935/REJP4030(7/31/2025), REJR1272(9/30/2025), REJS1196(10/31/2025), REJS4633(7/31/2025); 3194108D/00801741027727/REJP4058(7/31/2025), REJS1304(5/31/2025); CK000545/00801741107399/REJP4222(1/31/2027), REJQ2267(2/28/2027); 1174108D5/00801741155147/REJQ0781(5/31/2025), REJQ1423(6/30/2025), REJS2164(6/30/2025), REJT0678(7/31/2025); 3174108D/00801741027581/REJQ0800(8/31/2025), REJQ1341(8/31/2025), REJR2656(9/30/2025); CK000775A/00801741188060/REJQ0807(8/31/2025), REJR1435(9/30/2025), REJS4754(10/31/2025), REJT0896(9/30/2025); 1194108D5/00801741155192/REJQ1441(6/30/2025), REJR1268(8/31/2025), REJS2058(7/31/2025), REJS3889(7/31/2025), REJT0862(7/31/2025); CK000736/00801741139499/REJQ1480(6/30/2025); CK000739/00801741139659/REJQ1601(6/30/2025), REJR2683(6/30/2025), REJS3894(8/31/2025), REJU1681(8/31/2025), REJV0873(8/31/2025), REJV3827(1/31/2026); 9194108/00801741028595/REJR0580(9/30/2025); 1194108/)00801741034503/REJR0596(9/30/2025), REJR2204(9/30/2025), REJS3533(10/31/2025); CK000660/00801741129650/REJR1419(9/30/2025), REJS1312(9/30/2025); CK000609A/00801741222504/REJR1654(6/30/2025); 9174108D/00801741035555/REJR1668(9/30/2025), REJR2230(9/30/2025); CK001067/00801741228711/REJR2202(8/31/2025), REJS3899(10/31/2025); CK000077D/00801741139598/REJR2231(9/30/2025); CK000882/00801741188794/REJS0259(8/31/2025), REJT0908(11/30/2025); CK000874/00801741178696/REJS0282(7/31/2025), REJS2188(6/30/2025), REJT1411(11/30/2025); CK000994/00801741215698/REJS0285(7/31/2025), REJS3572(8/31/2025); CK000870A/00801741184246/REJS3569(10/31/2025); CK000443C/00801741226557/REJT0880(10/31/2025); CK000668B/00801741228674/REJT1820(10/31/2025); CK000784/00801741189012/REJU0379(9/30/2025)
Devices named in this recall
104 devices in the FDA device registry whose identifier appears in the recall's code information; the 100 most reported are shown.
- PowerPICC Catheter 3174118Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall402 reports
- PowerPICC SOLO2 Catheter 1194108DBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 recalls216 reports
- PowerPICC® Catheters 1174108DBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall222 reports
- PowerPICC 1174108D4Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 recalls70 reports
- PowerPICC SOLO 1194108D5Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 recalls58 reports
- PowerPICC 1174108D5Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 recalls53 reports
- PowerPICC SOLO 1194108D4Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 recalls32 reports
- PowerPICC 1174108D3Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 recalls24 reports
- PowerPICC CK000631BBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 recalls14 reports
- PowerPICC SOLO2 Catheter 3194108DBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 recalls10 reports
- PowerPICC SOLO2 Catheter with Sherlock Tip Location System (TLS) Stylet 9194108DBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 recalls10 reports
- PowerPICC SOLO 1194108D1Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 recalls10 reports
- PowerPICC Catheter with Sherlock 3CG Tip Positioning System (TPS) Stylet 1174118Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall55 reports
- PowerPICC CK000613Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 recalls5 reports
- PowerPICC SOLO CK000289CBard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days2 recalls5 reports
- PowerPICC SOLO CK000586BBard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days2 recalls1 report
- PowerPICC SOLO CK001030Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days2 recalls0 reports
- PowerPICC Catheter 3174155Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall26 reports
- PowerPICC SOLO 1194108D2Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall26 reports
- PowerPICC SOLO2 Catheter 3194355Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall25 reports
- PowerPICC SOLO 1194108D3Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall24 reports
- PowerPICC SOLO2 Catheter 3194335Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall18 reports
- PowerPICC SOLO2 Catheter with Sherlock Tip Location System (TLS) Stylet 9194118Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall18 reports
- PowerPICC® Catheter 3174335Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall15 reports
- PowerPICC Catheter with Sherlock 3CG Tip Positioning System (TPS) Stylet 1174108Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall15 reports
- PowerPICC CK000775ABard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall14 reports
- PowerPICC 1174108D2Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall13 reports
- PowerPICC Catheter 3174355Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall12 reports
- PowerPICC SOLO CK000930Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall12 reports
- PowerPICC SOLO2 Catheter 3194118Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall10 reports
- PowerPICC SOLO2 Catheter 3194155Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall10 reports
- PowerPICC® Catheter 3174108DBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall9 reports
- PowerPICC SOLO2 Catheter with Sherlock 3CG Tip Positioning System (TPS) Stylet 1194108Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall7 reports
- PowerPICC 1174108D1Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall7 reports
- PowerPICC CK000986Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall7 reports
- PowerPICC SOLO2 Catheter with Sherlock Tip Location System (TLS) Stylet 9194108Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall6 reports
- PowerPICC® Catheter 3174108Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall5 reports
- PowerPICC Catheter with Sherlock Tip Location System (TLS) Stylet 9174108DBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall5 reports
- PowerPICC SOLO CK000687Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall5 reports
- PowerPICC CK000819Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall5 reports
- PowerPICC CK000897Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall5 reports
- PowerPICC Catheter with Sherlock Tip Positioning System (TPS) Stylet 9174108Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall4 reports
- PowerPICC CK000677Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall4 reports
- PowerPICC SOLO CK000900Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall4 reports
- PowerPICC SOLO CK001027Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall4 reports
- PowerPICC Catheter 3174135Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall3 reports
- PowerPICC SOLO2 Catheter 3194135Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall3 reports
- PowerPICC CK000411Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall3 reports
- PowerPICC CK000513ABard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall3 reports
- PowerPICC SOLO CK000501ABard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall3 reports
- PowerPICC CK000870ABard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall3 reports
- PowerPICC Sherlock 3CG CK000668BBard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall3 reports
- PowerPICC SOLO2 Catheter 3194108Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall2 reports
- PowerPICC CK000060Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall2 reports
- PowerPICC SOLO CK000524ABard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall2 reports
- PowerPICC CK000739Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall2 reports
- PowerPICC CK000757Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall2 reports
- PowerPICC CK000881Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall2 reports
- PowerPICC CK000991Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall2 reports
- PowerPICC CK000196Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall1 report
- PowerPICC Catheter with Sherlock Tip Positioning System (TPS) Stylet 9174118Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall1 report
- PowerPICC CK000335ABard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall1 report
- PowerPICC CK000549Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall1 report
- PowerPICC SOLO CK000660Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall1 report
- PowerPICC SOLO CK000589ABard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall1 report
- PowerPICC CK000796Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall1 report
- PowerPICC CK000285CBard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall1 report
- PowerPICC SOLO CK000867Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall1 report
- PowerPICC CK000315ABard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall1 report
- PowerPICC SOLO CK000882Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall1 report
- PowerPICC SOLO CK000937ABard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall1 report
- PowerPICC CK000443CBard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall1 report
- PowerPICC CK000483Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall0 reports
- PowerPICC CK000445Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall0 reports
- PowerPICC CK000540Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall0 reports
- PowerPICC CK000545Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall0 reports
- PowerPICC CK000567Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall0 reports
- PowerPICC CK000617Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall0 reports
- PowerPICC SOLO CK000642Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall0 reports
- PowerPICC SOLO CK000619ABard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall0 reports
- PowerPICC SOLO CK000721Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall0 reports
- PowerPICC CK000736Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall0 reports
- PowerPICC SOLO CK000077DBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall0 reports
- PowerPICC CK000839Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall0 reports
- PowerPICC CK000844Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall0 reports
- PowerPICC SOLO CK000864Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall0 reports
- PowerPICC CK000874Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall0 reports
- PowerPICC CK000903Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall0 reports
- PowerPICC SOLO CK000266ABard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall0 reports
- PowerPICC CK000934Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall0 reports
- PowerPICC SOLO CK000894ABard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall0 reports
- PowerPICC CK000784Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall0 reports
- PowerPICC CK000955Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall0 reports
- PowerPICC CK000959Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall0 reports
- PowerPICC SOLO CK000914Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall0 reports
- PowerPICC SOLO CK000994Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall0 reports
- PowerPICC SOLO CK000609ABard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall0 reports
- PowerPICC CK001021Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall0 reports
- PowerPICC CK001018Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall0 reports
- PowerPICC CK000953ABard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall0 reports
Product lines
- PowerPICCBard Access Systems, Inc. · 118 models · 401 reports · 3 recalls
- PowerPICC SOLOBard Access Systems, Inc. · 78 models · 306 reports · 3 recalls
- PowerPICC SOLO2 CatheterBard Access Systems, Inc. · 20 models · 517 reports · 2 recalls
- PowerPICC CatheterBard Access Systems, Inc. · 33 models · 1,014 reports · 3 recalls
- PowerPICC Sherlock 3CGBard Access Systems, Inc. · 7 models · 6 reports · 2 recalls
- PowerPICC CathetersBard Access Systems, Inc. · 3 models · 354 reports · 2 recalls
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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