Bard recalls specific PowerPICC SV catheter models due to lidocaine ampoules being manufactured under deficient practices. Affected units have unique UDI-DI codes and lot numbers. Consumers should check their catheters for these identifiers.
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Bard is recalling two specific models of PowerPICC SV catheters because the lidocaine ampoules used in their production were made with poor manufacturing practices. This issue could lead to unsafe drug delivery if the ampoules are compromised.
The lidocaine ampoules in the catheters were manufactured under deficient practices, which could lead to improper drug delivery. However, the recall focuses on the ampoules rather than the catheters themselves being defective.
Patients using Bard PowerPICC SV catheters with the specific UDI-DI codes and lot numbers listed in the recall are affected. Healthcare providers administering these catheters are most at risk.
Check for the UDI-DI code (00801741087110 for 4-fr dual-lumen or 00801741027536 for 3-fr single-lumen) and lot number (REKW2449 or REKV2227) on the catheter packaging.
Look for the UDI-DI code and lot number on the catheter packaging to confirm if it's affected.
The lidocaine ampoules used in the catheters were manufactured under deficient practices, which could affect drug delivery safety.
Check the UDI-DI code and lot number on the packaging to see if it's affected. If it is, contact Bard for further instructions.
The recall is due to manufacturing issues with the lidocaine ampoules, not the catheters themselves. The risk is low as the issue is specific to the ampoules.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-2659-2026 — Bard Bard Hello, I own a Bard that is covered by recall Z-2659-2026 from Bard. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
