ARROW recallZ-2376-2026 · Arrow International, LLC · initiated Apr 21, 2026

Why it was recalled

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.

FDA root cause category: Nonconforming Material/Component

What the company is doing

On 4/21/2026, correction notices (Firm Event Number: EIF-000608, lidocaine and bupivacaine) were mailed to customers who were asked to do the following: Arrow International LLC is voluntarily recalling product due to the Huons Co. Ltd. recall of Lidocaine and Bupivacaine, which is included in impacted Arrow Kits & Sets. Medical facilities 1. Provide this correction notice to all persons who need to be aware within your organization or to any organization where the potentially affected product has been transferred. 2. Check your inventory for product within the scope of this Medical Device Notification and place a copy of this notice with all affected product. 3. Complete and return the response form virtually via: https://fca.myteleflex.com/en/recall/000608 Distributors: 1. Provide Medical Device Notification to all customers who have received impacted product. Each of your customers is then required to complete the Acknowledgement Form and return it to you as their distributor. 2. Check your inventory for affected product. Place a copy of this notification with all affected product and ensure that the notification is included with future distributions of affected product. 3. Complete and return the response form via link: https://fca.myteleflex.com/en/recall/000608 4. If you have further distributed product outside of your country, please notify Teleflex Customer Service by return email. If you have questions contact firm's Customer Service: Link: https://fca.myteleflex.com/en/recall/000608, Customer Service: Telephone: 1-866-396-2111, FAX: 1-855-419-8507 Email: [email protected] On 5/29/2026, additional amended notices (Firm Event Number: EIF-000608-01) were mailed to include additional affected devices. On 5/1/2026, additional notices (Firm Event Number: EIF-000609, sodium chloride) were mailed and emailed to customers who have 0.9% sodium chloride (10mL saline solution ampule) in kits and sets.

Recall details

Recall number

Z-2376-2026

Recall class

Class I (most serious)

Status

Open, Classified

Initiated by the company

Apr 21, 2026

Posted by the FDA

Jun 13, 2026

Recalling firm

Arrow International, LLC

Quantity

308,263

Product code

LRS

FDA submissions

K071538, K900263, K970864, K993691

Distribution

US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.

Product description

Description/REF: CVC/PSI KIT: 2 LUMEN 8 FR X 6 IN/ASK-42802-PLH; CVC KIT: 3-LUMEN 12 FR X 16 CM/AK-12123-F; CVC KIT: 3-LUMEN 12 FR X 20 CM/AK-15123-F; 3L CVC KIT: 7 FR X 16 CM/ASK-12703-PMAH; 3L PI CVC KIT: 7 FR X 16 CM/ASK-12703-PNM; 3L CVC KIT: 7 FR X 16 CM/ASK-12703-PUMH; MULTILUMEN PI CVC KIT: 3L 7 FR X 8 IN/ASK-15703-PRH; MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/CDC-15703-P1A; PI CVC KIT: 3-L 7 FR X 6IN (16 CM)/NA-12703-PCDC; PI CVC KIT: 3-L 7 FR X 8IN (20 CM)/NA-15703-PCDC; CVC KIT: 3-LUMEN 5.5 FR X 8 CM/AK-25553; 2-L CVC KIT: 4 FR X 5 CM/CDC-22402-X1A; 2-L CVC KIT: 5 FR X 5 CM/CDC-22502-X1A; 2-L CVC KIT: 4 FR X 8 CM/CDC-25402-X1A; 2-L CVC KIT: 5 FR X 8 CM/CDC-25502-X1A; 3-L CVC KIT: 5.5 FR X 8 CM/CDC-25553-X1A; 3-L CVC KIT: 5.5 FR X 13 CM/CDC-26553-X1A; CVC KIT 3L: 12 FR X 16 CM AGB/AK-22123-CDC; CVC KIT: 3-LUMEN 12 FR X 16 CM/AK-22123-F; CVC KIT: 2-LUMEN 4 FR X 5 CM/AK-22402; CVC KIT: 2-LUMEN 5 FR X 5 CM/AK-22502; CVC KIT: 16 GA X 8IN/AK-24301-SK; CVC KIT: 2-LUMEN 4 FR X 13 CM/AK-24402; CVC KIT: 3-LUMEN 7 FR X 30 CM/AK-24703-ASK; CVC KIT 3L: 12FR X 20 CM AGB/AK-25123-CDC; CVC KIT: 3-LUMEN 12 FR X 20 CM/AK-25123-F; CVC KIT: 2-LUMEN 4 FR X 8 CM/AK-25402; CVC KIT: 2-LUMEN 5 FR X 8 CM/AK-25502; CVC KIT: 3-LUMEN 5.5 FR X 13 CM/AK-26553; LBCVC KIT: 3L 12 FR X 16 CM AGB/CDC-22123-1A; LBCVC KIT: 3L 12 FR X 16 CM AGB/CDC-22123-X1A; CVC KIT: 16 GA X 20 CM/CDC-24301-1A; PI CVC KIT: 2L 7 FR X 16 CM AGB/AK-22702-P1A; PI CVC KIT: 2L 7 FR X 16 CM AGB/CDC-22702-XP1A; CVC KIT: 3L 7 FR X 20 CM/ASK-45703-CPR; MULTILUMEN PI CVC KIT: 3L 7 FR X 16 CM/ASK-42703-AKP1A; MULTI-LUMEN PI CVC KIT: 3-L 7 FR X 6IN/ASK-42703-KH; PI CVC KIT: 3L 7FR X 16CM AGB+/ASK-42703-MGH1; MULTI LUMEN PI CVC KIT: 3L 7 FR X 6IN/ASK-42703-PCCH2; PI CVC KIT: 3LUMEN 7 FR X 6IN (16 CM)/ASK-42703-PFS1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PNO2; MULTI LUMEN PI CVC KIT: 3L 7 FR/ASK-42703-PSCH1; MULTILUMEN PI CVC KIT: 2L 8 FR X 16 CM/ASK-42802-AKP1A; CVC KIT: 2L 8 FR X 16CM/ASK-42802-LMDTG1; PI CVC KIT: 2L 8 FR X 6 IN (16 CM) AGB+/ASK-42802-PUCI1; PI CVC KIT: 2L 8 FR X 16 CM AGB+/ASK-42802-PUMH; PI CVC KIT: 2L 8 FR X 16 CM AGB+/ASK-42802-UMM; PI CVC KIT: 4-L 8.5 FR X 6 IN/ASK-42854-AKP1A; PI CVC KIT: 4L 8.5FR X 16CM AGB+/ASK-42854-MGH; MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-AKP1A; PI CVC KIT: 3L 7 FR X 20CM AGB+/ASK-45703-MGH; MULTI LUMEN PI CVC KIT: 3L 7 FR X 8 IN/ASK-45703-PCCH2; MULTI LUMEN PI CVC KIT: 3L 7 FR X 8 IN/ASK-45703-PECL1; PI CVC KIT: 3 LUMEN 7 FR X 8 IN (20 CM)/ASK-45703-PFS1; PI CVC KIT: 3L 7 FR X 8 IN (20 CM) AGB+/ASK-45703-PHM1; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-PHU; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-PMSG1; MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PNCB; MULTILUMEN CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PPCM; PI CVC KIT: 3-LUMEN 7 FR X 8 IN (20 CM)/ASK-45703-PRH; MULTILUMEN PI CVC KIT: 3L 7 FR X 8 IN/ASK-45703-PSJ2; PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PSVM; MULTI LUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PUHS; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-PUKL; PI CVC KIT: 3L 7FR X 20CM AGB+/ASK-45703-PUMF1; PI CVC KIT: 3L 7 FR X 8 IN (20 CM)/ASK-45703-PUR1; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-RHR1; MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-WA; MULTI LUMEN PI CVC KIT: 2L 8 FR X 8 IN/ASK-45802-AKP1A; PI CVC KIT: 4L 8.5 FR X 20 CM/ASK-45854-AKP1A; PI CVC KIT: 4L 8.5FR X 20CM AGB+/ASK-45854-MGH; PI CVC KIT: 4L 8.5 FR X 8IN/ASK-45854-PCCH2; CVC KIT: 4L 8.5 FR X 20 CM AGB/ASK-45854-PNM; MULTI LUMEN CVC KIT: 4L 8.5 FR X 8 IN/ASK-45854-PPCM; PI CVC KIT: 4L 8.5 FR X 20 CM AGB+/ASK-45854-PUCH2; MULTILUMEN PI CVC KIT: 2L 7 FR X 20 CM/ASK-46702-PWBH1; MULTILUMEN CVC KIT: 2L 8 FR X 16 CM/CDC-42802-P1A; PI CVC KIT: 3-L 7 FR X 20 CM AGB/CDC-45703-PA1A; CVC KIT: 2L 8 FR X 6IN (16 CM)/ASK-42802-ECL4; PI CVC KIT: 3-L 7 FR X 16 CM AGB+/AK-42703-P1A; PI CVC KIT: 2-L 8 FR X 16 CM AGB+/AK-42802-P1A; PI CVC KIT: 4-L 8.5 FR X 16 CM AGB+/AK-42854-P1A; PI CVC KIT: 3-L 7 FR X 20 CM AGB+/AK-45703-P1A; PI CVC KIT: 2-L 8 FR X 20 CM AGB

Devices named in this recall

87 devices in the FDA device registry whose identifier appears in the recall's code information.

• ARROW IPN925037

  Teleflex Incorporated · CATHETER, CONDUCTION, ANESTHETIC
  7 recalls0 reports
• ARROW IPN038522

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  3 recalls1 report
• ARROW IPN931283

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  3 recalls0 reports
• ARROW IPN931284

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  3 recalls0 reports
• ARROW IPN931286

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  3 recalls0 reports
• ARROW IPN036445

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  2 recalls8 reports
• ARROW IPN915628

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls5 reports
• ARROW IPN916994

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls4 reports
• ARROW IPN036830

  Teleflex Incorporated · INTRODUCER, CATHETER
  2 recalls3 reports
• ARROW IPN036452

  Teleflex Incorporated · INTRODUCER, CATHETER
  2 recalls3 reports
• ARROW IPN915630

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls2 reports
• ARROW IPN036474

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  2 recalls1 report
• ARROW IPN904896

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  2 recalls1 report
• ARROW IPN038523

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls1 report
• ARROW IPN923102

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls1 report
• ARROW IPN927593

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls1 report
• ARROW IPN036596

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  2 recalls0 reports
• ARROW IPN037185

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  2 recalls0 reports
• ARROW IPN037016

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  2 recalls0 reports
• ARROW IPN037790

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  2 recalls0 reports
• ARROW IPN055589

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls0 reports
• ARROW IPN915625

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls0 reports
• ARROW IPN056570

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls0 reports
• ARROW IPN916803

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls0 reports
• ARROW IPN917020

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls0 reports
• ARROW IPN917026

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls0 reports
• ARROW IPN919358

  Teleflex Incorporated · Catheter, hemodialysis, triple lumen, non-implanted
  2 recalls0 reports
• ARROW IPN922680

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls0 reports
• ARROW IPN922682

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls0 reports
• ARROW IPN923103

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls0 reports
• ARROW IPN927740

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls0 reports
• ARROW IPNB00178

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls0 reports
• ARROW IPNB00181

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls0 reports
• ARROW IPNB00182

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls0 reports
• ARROW IPNB00180

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls0 reports
• ARROW IPN036428

  Teleflex Incorporated · CATHETER, HEMODIALYSIS, NON-IMPLANTED
  2 recalls0 reports
• ARROW IPN036437

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  1 recall33 reports
• ARROW IPN927331

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall3 reports
• ARROW IPN037257

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  1 recall1 report
• ARROW IPN037093

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  1 recall1 report
• ARROW IPN036540

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  1 recall1 report
• ARROW IPN036988

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  1 recall1 report
• ARROW IPN036502

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  1 recall0 reports
• ARROW IPN036534

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  1 recall0 reports
• ARROW IPN036601

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  1 recall0 reports
• ARROW IPN036495

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  1 recall0 reports
• ARROW IPN036566

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  1 recall0 reports
• ARROW IPN037155

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  1 recall0 reports
• ARROW IPN037069

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  1 recall0 reports
• ARROW IPN037166

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  1 recall0 reports
• ARROW IPN037691

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  1 recall0 reports
• ARROW IPN038176

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  1 recall0 reports
• ARROW IPN029652

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN055555

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN914810

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN055840

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN056641

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN916989

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN916991

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN916996

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN916812

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN916813

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN916816

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN916818

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN916819

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN916836

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN917104

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN917373

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN917134

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN917135

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN916995

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN919342

  Teleflex Incorporated · Catheter, hemodialysis, triple lumen, non-implanted
  1 recall0 reports
• ARROW IPN923110

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN926612

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN927330

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN928775

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN931285

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPNB00080

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPNB00093

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN036512

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  1 recall0 reports
• ARROW IPN036454

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  1 recall0 reports
• ARROW IPN036510

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN036493

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  1 recall0 reports
• ARROW IPN036468

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  1 recall0 reports
• ARROW IPN037015

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN037130

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall0 reports
• ARROW IPN036961

  Teleflex Incorporated · Catheter, hemodialysis, triple lumen, non-implanted
  1 recall0 reports

Product lines

• ARROWTeleflex Incorporated · 1,494 models · 9,043 reports · 62 recalls

Other devices under the same FDA submission

231 devices cleared under K071538, K900263, K970864, K993691 are not named by identifier in this recall. One submission often covers many models, so they may or may not be affected.

• ARROW IPN030177

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  254 reports
• ARROW IPN030162

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  163 reports
• ARROW IPN055818

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls1 report
• ARROW IPN055820

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls1 report
• ARROW IPN056571

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls1 report
• ARROW IPN917372

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls1 report
• ARROW IPN055870

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls0 reports
• ARROW IPN056182

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls0 reports
• ARROW IPN922908

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  2 recalls0 reports
• Medline Industries, Inc. DYNDM1031A

  Medline Industries, Inc. · Catheter,intravascular,therapeutic,short-term less than 30 days
  2 recalls0 reports
• ARROW IPN915614

  Teleflex Incorporated · Catheter, intravascular, therapeutic, short-term less than 30 days
  1 recall48 reports
• ARROW IPN030129

  Teleflex Incorporated · Catheter,intravascular,therapeutic,short-term less than 30 days
  71 reports

Other products in the same recall event

The FDA groups related products into one recall event (event 98793).

• Z-2363-2026 · Open, Classified
  PARACENTESIS KIT, REF: AK-00376, ASK-00376-VCU
• Z-2364-2026 · Open, Classified
  Description/REF: ACCESS TRAY/ASK-04001-SUH-S; ACCESS TRAY/ASK-04001-VM1; STIMUCATH SFTY KIT: 19G CTH, 17Gx4CM NDL/AB-19604-KS; STIMUCATH SFTY KIT: 19G CTH, 17Gx8CM NDL/AB-19608-KS;…
• Z-2365-2026 · Open, Classified
  Description/REF: BIOPSY SYSTEM COMPREHENSIVE KIT/ASK-09458-AH, ASK-09458-COC, ASK-09458-EUH, ASK-09458-SD, ASK-09458-VU
• Z-2366-2026 · Open, Classified
  Description/REF: PACING PSI KIT: 6 FR/AI-06210-KS, PACING PSI KIT: 5 FR 2-L/AI-07155-KS, PACING PSI KIT: 5 FR 2L/ASK-07155-UPM
• Z-2367-2026 · Open, Classified
  Description/REF: AGBA PICC G4 Stylet: 3L 6FR x 55CM BP/DLX-45563-VPSB; AGBA PICC G4 Stylet: 3L 6FR x 55CM TCG/DLX-45563-VPSC; ARROW(R) VPS(R) ACCESS KIT/ASK-04001-UCHD1; ARROW(R) V…
• Z-2368-2026 · Open, Classified
  Description/REF: RA CATH KIT: 20 GA X 1 3/4 IN/TJ-04020-1; RA CATH KIT: 20 GA X 1 1/2IN/NA-04220-S1A; ARTERIAL LINE KIT/AK-04510-S; ARTERIAL CATH KIT: 18 GA X 6IN (16 CM)/ASK-04018…
• Z-2369-2026 · Open, Classified
  Description/REF: PSI KIT: 7 FR X 4IN ANTIMICROBIAL/ASK-09701-UMH; PSI KIT: 8.5 FR X 4 1/8 IN (10 CM)/ASK-09803-OSU4; PSI/CVC KIT: 9 FR/7 FR X 6IN (16CM)/ASK-09903-AMC1; PSI KIT: 9 …
• Z-2370-2026 · Open, Classified
  Description/REF: PI AGBA PICC KIT: 3L 6 FR X 40 CM W/VPS/ASK-44063-NS AGBA PICC/DELTA: 2L 5.5 FR X 50 CM/ASK-45052-NS AGBA PICC/DELTA KIT: 1L 4.5 FR X 55 CM/ASK-45541-MHBV PICC KIT…
• Z-2371-2026 · Open, Classified
  Description/REF: EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05502-VM1; EPIDURAL CATHETERIZATION KIT: 19 GA/AK-05501; EPIDURAL CATHETERIZATION KIT/AK-05502; EPIDURAL CATHETERIZATION K…
• Z-2372-2026 · Open, Classified
  Description/REF: HEMODIALYSIS KIT: 2L 14 FR X 20 CM AGB CDC-25142-X1A
• Z-2373-2026 · Open, Classified
  Description/REF: HEMODIALYSIS KIT: 2-LUMEN 8 FR X 11 CM/AK-11802-F; HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-22122; HEMODIALYSIS KIT 2L: 14 FR X 15CM AGB/AK-22142-CDC; HEMODIALYS…
• Z-2374-2026 · Open, Classified
  Description/REF: AHDC KIT: 3-L 12 FR X 16 CM/AK-12123-PCDC; AHDC KIT: 3-L 12 FR X 20 CM/AK-15123-PCDC; AHDC KIT: 3-L 12 FR X 20 CM/CDC-15123-XP1A; AHDC KIT: 3-L 12 FR X 25 CM/CDC-1…
• Z-2377-2026 · Open, Classified
  Description/REF: ARTERIAL LINE KIT: SL 20 GA X 5 IN/ASK-04510-MM6 RA CATH KIT: 20 GA X 1-3/4IN/NA-04020-X1ASP ACCESS TRAY/ASK-04001-MS RA CATH KIT: 20 GA X 8 CM/ASK-00820-UM1 VESSE…
• Z-2378-2026 · Open, Classified
  Description/REF: PI PICC: 3: 6FR x 55CM w CHG/ DLX-35563-HPKC; AGBA PICC: 2L 5.5 FR X 45 CM/ASK-44552-ABKB; AGBA PICC/DELTA KIT: 5.5 FR X 55 CM/ASK-45552-MHBV; AGBA PICC: 1L 4.5FR …
• Z-2379-2026 · Open, Classified
  Description/REF: PI JACC KIT: 2L 5.5 FR X 15 CM CG+/ASK-41552-LTAC; PI JACC KIT: 3L 6 FR X 20 CM CG+/ASK-42063-LTAC; AGBA PI JACC KIT: 1-L 4.5 FR X 15 CM/CDC-41541-JX1A; AGBA PI JA…
• Z-2380-2026 · Open, Classified
  Description/REF: PERITONEAL LAVAGE CATH KIT:8FR/AK-09000
• Z-2381-2026 · Open, Classified
  Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-12122-F
• Z-2382-2026 · Open, Classified
  Description/REF: DRAINAGE KIT/AK-01600, DRAINAGE KIT/AK-01601, DRAINAGE KIT/ASK-01601-MM, THORACENTESIS KIT/AK-01000-T, THORACENTESIS KIT/AK-01000, THORACENTESIS KIT/ASK-01000-CHP,…
• Z-2383-2026 · Open, Classified
  Description/REF: PACING/PSI KIT: 5 FR 2L/ASK-07155-MGU
• Z-2384-2026 · Open, Classified
  Description/REF: ACCESS TRAY/ASK-04001-JHH; ACCESS TRAY/ASK-04001-LMDTG; PI CVC KIT: 3 LUMEN 7 FR X 6 IN (16 CM)/ASK-12703-PSPH1; 3L CVC KIT: 7 FR X 16 CM/ASK-12703-WMC2; MULTILUME…
• Z-2385-2026 · Open, Classified
  Description/REF: ACCESS TRAY/GU-04020; PSI KIT: 8.5 FR/AK-09803-CDC; PSI KIT: 9 FR/AK-09903-CDC; PSI KIT: 8.5 FR X 4 IN (10 CM)/ASK-09810-PCMH1; PSI KIT: 9 FR X 10 CM/ASK-09903-KH;…
• Z-2387-2026 · Open, Classified
  Description/REF: PI MIDLINE 2L: 5FR X 20CM/CDC-32052-MPKC
• Z-2388-2026 · Open, Classified
  Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 20 CM/AK-15122-F, AHDC KIT: 3L 12 FR X 16 CM/ASK-12123-UOC1, AHDC KIT: 3-L 12 FR X 16 CM/ASK-12123-UPM, AHDC KIT: 3L 12 FR X 20 C…
• Z-2389-2026 · Open, Classified
  Description/REF: SPINAL ANESTHESIA KIT/ASA-24090-SB; SPINAL ANESTHESIA KIT/ASA-24103-SB; SPINAL ANESTHESIA KIT/ASA-25090-SB; SPINAL ANESTHESIA KIT: 24 GA X 9 CM/ASK-24090-SA; SPINA…
• Z-2390-2026 · Open, Classified
  Description/REF: SAC KIT: 18 GA X 12CM W BIO/SAC-01218-B; SAC KIT: 18 GA X 12CM W CHG/SAC-01218-C; SAC KIT: 18 GA X 16CM W BIO/SAC-01618-B
• Z-2391-2026 · Open, Classified
  Description/REF: RA CATH KIT: 20 GA X 1-3/4IN/AK-04020-SPC; RA CATH KIT: 20 GA X 5 IN/ASK-04020-MW; ARTERIAL LINE KIT: SL 20 GA X 5 IN/ASK-04510-MM5; CATH SL 20 GA X 5 CM HYDROPHIL…
• Z-2393-2026 · Open, Classified
  Description/REF: PSI KIT: 7 FR X 4 IN/ASK-09701-UP; PSI KIT: 8.5 FR X 4 1/8 IN (10 CM)/ASK-09803-OSU5; PSI KIT: 8.5 FR/ASK-09807-UC; PSI KIT: 9 FR X 4 1/8IN (10 CM)/ASK-09903-HH2; …
• Z-2394-2026 · Open, Classified
  Description/REF: MIDLINE CATHETER KIT: 3 FR X 20 CM/CDC-02031-MK1A; AM/AT PI MIDLINE 1L: 4.5FR X 15CM/CDC-41541-MPK1A; AM/AT PI MIDLINE 2L: 5.5FR X 15CM/CDC-41552-MPK1A; AGBA PI MI…
• Z-2396-2026 · Open, Classified
  Description/REF: CVC KIT: 16 GA X 8IN/AK-04210, CVC KIT: 1-L 16 GA X 8IN (20 CM)/AK-04300, CVC KIT: 14 GA X 6 IN/CK-04711
• Z-2397-2026 · Open, Classified
  Description/REF: RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-1A; RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-X1A; ARTERIAL CATHETER KIT: 18 GA X 16 CM/ASK-04018-HCA; ARTERIAL CATHETER KIT: 18 …