1174108 PowerPICC Catheter 4 Fr Single-Lumen recallZ-2666-2026 · Bard Access Systems, Inc. · initiated May 21, 2026
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
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
FDA root cause category: Nonconforming Material/Component
What the company is doing
On 05/21/2026, the firm FedEx'd an "URGENT: Medical Device Recall" letter informing customers/distributed that BD has become aware that the FDA has placed Lidocaine manufactured by Huons Co., Ltd. on import alert #66-40 - Detention Without Physical Examination of Drugs From Firms Which Have Not Met Drug GMPs. BD is recalling products that contain the affected lidocaine ampules. Customers are instructed to: 1. Not to use the affected Lidocaine ampules. 2. Secure an alternative local Lidocaine drug prior to entering the procedural environment. 3. Upon opening the kit, remove and destroy the drug product from the BD convenience kits/procedure trays at the point of use, within a controlled and sterile environment to maintain the sterility of the remaining components within the kit. All other kit/tray components are safe to use. 4. If affected Lidocaine ampule was previously used without issue, no additional treatment or clinical follow up is required. 5. If affected Lidocaine ampule was previously used with issue, report the incident per institutional guidelines and take any necessary actions. Additional actions to take: 1. Circulate this notice to all those who need to be aware within your organization or to any organization where the potentially affected products have been transferred. 2. Post this notice on all inventory storage locations and any location where the product may be used. 3. Label affected kits/trays using the template provided in Appendix 2 to facilitate easy identification of products containing the affected ampules. The label can be printed using Avery template 5160. a. Apply the labels to the product without covering or obscuring any regulatory or traceability information. b. Apply to the top web of the kit/tray pressing firmly to ensure adhesion, while taking care not to damage or compromise the sterile barrier. For Questions - Contact North American Regional Complaint Center at 1-844-8BD-LIFE (1-844-823-5433) Say Product Complaints when prompt
Recall details
- Recall number
- Z-2666-2026
- Status
- Open, Classified
- Initiated by the company
- May 21, 2026
- Posted by the FDA
- Jul 2, 2026
- Recalling firm
- Bard Access Systems, Inc.
- Quantity
- 39,245
- Product code
- LJS
- FDA submissions
- K210264
- Distribution
- Worldwide U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, and WY. The country of Belgium.
Product description
1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 1295108 PowerPICC SOLO Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741034602 1174108D3 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 1174108D4 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741155048 1174108D5 PowerPICC Catheter 4 Fr Singel-Lumen UDI-DI Code: 00801741155147 1194108D PowerPICC SOLO Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741034510 1194108D1 PowerPICC SOLO Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154782 1194108D4 PowerPICC SOLO Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741155093 1194108D5 PowerPICC SOLO Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741155192 1275108D PowerPICC Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741034558 1295108FD PowerPICC SOLO FT Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741034626 3194108D PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741027727 3275108D PowerPICC Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741027871 3295108D PowerPICC SOLO FT Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741028052 9194108D PowerPICC SOLO Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741035609 CK000267A PowerPICC SOLO2 Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741185021 CK000289C PowerPICC SOLO Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741161148 CK000293 PowerPICC HF Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741038020 CK000586B PowerPICC SOLO Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741212789 CK000613 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121395 CK000631B PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741143748 CK000632B PowerPICC Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741143755 CK000746A PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741227066 CK000886 PowerPICC Provena Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741188831 CK000966A PowerPICC Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741215858 CK000988 PowerPICCProvena Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741216022 CK001006 PowerPICC Provena Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741219849 CK001030 PowerPICC SOLO Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741223976 S1275108FD2 PowerPICC Provena FT Catheter 5 Fr Dual-Lumen UDI-Di Code: 00801741154850 S1275108FD3 PowerPICC Provena FT Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741154959 S1295108FD1 PowerPICC Provena Catheter SOLO 5 Fr Dual-Lumen UDI-DI Code: 00801741154805 S1295108FD3 PowerPICC Provena SOLO FT Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741155017 S1295108FD5 PowerPICC Provena SOLO FT Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741155215 S1385108D PowerPICC Provena Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741112720 S1385108D2 PowerPICC Provena Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741154867 S1385108D3 PowerPICC Provena Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741154966 S1385108D4 PowerPICC Provena Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741155079 S1395108D PowerPICC Provena SOLO Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741112751 S1395108D1 PowerPICC Provena SOLO Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741154812 S1395108D2 PowerPICC Provena SOLO Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741154911 S1395108D3 PowerPICC Provena SOLO Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741155024 S1395108D4 PowerPICC Provena SOLO Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741155123 S1395108D5 PowerPICC Provena SOLO Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741155222
Code information (models, lots, serial numbers)
Show the full code information (4k characters)
1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 Lot Numbers: REKW0930 REKX0625 1295108 PowerPICC SOLO Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741034602 Lot Number: REKX2233 1174108D3 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 Lot Number: REKW2495 1174108D4 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741155048 Lot Number: REKW0912 1174108D5 PowerPICC Catheter 4 Fr Singel-Lumen UDI-DI Code: 00801741155147 Lot Number: REKW0980 1194108D PowerPICC SOLO Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741034510 Lot Number: REKW2454 1194108D1 PowerPICC SOLO Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154782 Lot Number: REKX0643 1194108D4 PowerPICC SOLO Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741155093 Lot Number: REKW1471 1194108D5 PowerPICC SOLO Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741155192 Lot Number: REKY0121 1275108D PowerPICC Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741034558 Lot Number: REKW0913 1295108FD PowerPICC SOLO FT Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741034626 Lot Numbers: REKP1491 REKW1478 REKX0051 3194108D PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741027727 Lot Numbers: REKW0937 REKX0095 3275108D PowerPICC Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741027871 Lot Number: REKP0933 3295108D PowerPICC SOLO FT Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741028052 Lot Numbers: REKN0696 REKW0451 9194108D PowerPICC SOLO Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741035609 Lot Number: REKW2499 CK000267A PowerPICC SOLO2 Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741185021 Lot Number: REKU2372 CK000289C PowerPICC SOLO Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741161148 Lot Number: REKP0950 CK000293 PowerPICC HF Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741038020 Lot Number: REKN2100 CK000586B PowerPICC SOLO Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741212789 Lot Number: REKY1980 CK000613 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121395 Lot Number: REKX0904 CK000631B PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741143748 Lot Number: REKW2466 CK000632B PowerPICC Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741143755 Lot Number: REKX3758 CK000746A PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741227066 Lot Number: REKX1896 CK000886 PowerPICC Provena Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741188831 Lot Number: REKW2474 CK000966A PowerPICC Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741215858 Lot Number: REKP0918 CK000988 PowerPICCProvena Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741216022 Lot Numbers: REKW0468 REKX2706 CK001006 PowerPICC Provena Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741219849 Lot Number: REKX0941 CK001030 PowerPICC SOLO Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741223976 Lot Number: REKY1950 S1275108FD2 PowerPICC Provena FT Catheter 5 Fr Dual-Lumen UDI-Di Code: 00801741154850 Lot Number: REKX0671 S1275108FD3 PowerPICC Provena FT Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741154959 Lot Number: REKX0661 S1295108FD1 PowerPICC Provena Catheter SOLO 5 Fr Dual-Lumen UDI-DI Code: 00801741154805 Lot Number: REKW1459 S1295108FD3 PowerPICC Provena SOLO FT Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741155017 Lot Number: REKW1476 S1295108FD5 PowerPICC Provena SOLO FT Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741155215 Lot Number: REKW0911 S1385108D PowerPICC Provena Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741112720 Lot Number: REKW0473 S1385108D2 PowerPICC Provena Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741154867 Lot Number: REKX0641 S1385108D3 PowerPICC Provena Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741154966 Lot Number: REKW1470 S1385108D4 PowerPICC Provena Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741155079 Lot Number: REKW2521 S1395108D PowerPICC Provena SOLO Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741112751 Lot Number: REKW2446 S1395108D1 PowerPICC Provena SOLO Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741154812 Lot Number: REKW0475 S1395108D2 PowerPICC Provena SOLO Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741154911 Lot Numbers: REKW2522 REKX2212 S1395108D3 PowerPICC Provena SOLO Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741155024 Lot Number: REKX2224 S1395108D4 PowerPICC Provena SOLO Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741155123 Lot Number: REKX0073 S1395108D5 PowerPICC Provena SOLO Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741155222 Lot Number: REKX0144
Devices named in this recall
42 devices in the FDA device registry whose identifier appears in the recall's code information.
- PowerPICC SOLO2 Catheter 1194108DBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 recalls216 reports
- PowerPICC SOLO2 Catheter 1295108DBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall125 reports
- PowerPICC 1174108D4Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 recalls70 reports
- PowerPICC® Catheters 1275108DBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall115 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 Provena S1395108DBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall75 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 SOLO2 FT Catheter 1295108FDBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall57 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 Provena SOLO S1395108D5Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall39 reports
- PowerPICC Provena S1385108DBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall38 reports
- PowerPICC Provena SOLO S1395108D2Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall32 reports
- PowerPICC Provena SOLO S1395108D3Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall28 reports
- PowerPICC Provena SOLO S1395108D4Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall27 reports
- PowerPICC Provena S1385108D4Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall22 reports
- PowerPICC Provena SOLO S1295108FD3Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall12 reports
- PowerPICC Provena SOLO S1295108FD5Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall11 reports
- PowerPICC Provena S1275108FD2Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall8 reports
- PowerPICC CK000632BBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall7 reports
- PowerPICC Provena S1385108D3Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall7 reports
- PowerPICC Provena S1275108FD3Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall6 reports
- PowerPICC® Catheter 3275108DBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall5 reports
- PowerPICC Provena CK000988Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall5 reports
- PowerPICC Provena SOLO S1295108FD1Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall4 reports
- PowerPICC Provena SOLO S1395108D1Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall4 reports
- PowerPICC Provena S1385108D2Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall4 reports
- PowerPICC Provena CK000886Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall4 reports
- PowerPICC SOLO2 Catheter 3295108DBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall2 reports
- PowerPICC CK000293Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall2 reports
- PowerPICC SOLO CK000267ABard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall1 report
- PowerPICC Provena CK001006Bard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall1 report
- PowerPICC CK000966ABard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall0 reports
- PowerPICC Sherlock 3CG CK000746ABard Access Systems, Inc. · Catheter, intravascular, therapeutic, long-term greater than 30 days1 recall0 reports
Product lines
- PowerPICC ProvenaBard Access Systems, Inc. · 116 models · 1,337 reports · 2 recalls
- PowerPICCBard Access Systems, Inc. · 118 models · 401 reports · 3 recalls
- PowerPICC Provena SOLOBard Access Systems, Inc. · 19 models · 201 reports · 2 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
Other products in the same recall event
The FDA groups related products into one recall event (event 99096).
- Z-2656-2026 · Open, ClassifiedCK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 CK000566 Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741108051 CK000566 Poly Midline C…
- Z-2657-2026 · Open, Classified5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code: 00801741042119 The intended use of the Short-Term Dialysis Catheter is attaining temporary/sh…
- Z-2658-2026 · Open, ClassifiedCK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741129674 Catheter stylets provide internal reinforcement to aid in catheter placement.
- Z-2659-2026 · Open, Classified1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 00801741087110 3173108D PowerPICC SV Catheter 3 Fr Single-Lumen REKV2227 00801741027536 The PowerPlCC SV catheters are in…
- Z-2660-2026 · Open, Classified5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Code: 00801741086953 5605240 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Tr…
- Z-2661-2026 · Open, Classified5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr Triple-Lumen UDI-DI Code: 00801741107177 5855300 Power-Trialysis Slim-Cath Straight Short-Term Dialys…
- Z-2662-2026 · Open, ClassifiedCK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138478 CK000729 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138713 P4153108D PowerMidline C…
- Z-2663-2026 · Open, ClassifiedCK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150 P4254108 PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741129278 P4254108D PowerMidline Cath…
- Z-2664-2026 · Open, ClassifiedCK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236129 CK000883 PowerPICC Provena Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188800 CK000884A Po…
- Z-2667-2026 · Open, ClassifiedCK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188770 S4153108BDP Provena Midline Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741154003 S4153108BP Proven…
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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