Bard recalls specific Provena Midline Catheters due to lidocaine ampoules manufactured under deficient practices. Affected units have UDI-DI codes and lot numbers listed. Consumers should check their catheters against the provided details.
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Bard is recalling specific models of Provena Midline Catheters because lidocaine ampoules used in their production were made under deficient manufacturing practices. This recall affects patients using these catheters for intravenous therapies or blood sampling, as the issue could lead to potential harm from improper drug delivery.
The recall is due to lidocaine ampoules being manufactured under deficient practices by the supplier. This could lead to improper drug delivery or contamination, potentially causing harm to patients during medical procedures.
Patients using Bard Provena Midline Catheters for intravenous therapies, blood sampling, or contrast media injections are most at risk. Healthcare providers who have these catheters in their inventory may also be affected.
Check for the UDI-DI codes and lot numbers listed in the recall notice: 00801741188770, 00801741154003, 00801741153990, 00801741153952, 00801741233258, 00801741154027, 00801741154140, 00801741154164, 00801741154119, 00801741233234, 00801741154188, 00801741185052, 00801741185069. The lot numbers include REKN2105, REKW2429, REKX1484, etc.
Compare your catheter's UDI-DI code and lot number with the list provided in the recall notice to determine if it is affected.
The recall is due to lidocaine ampoules being manufactured under deficient practices by the supplier, which could lead to improper drug delivery or contamination.
Check your catheter's UDI-DI code and lot number against the list provided in the recall notice, which includes specific codes like 00801741188770 and lot numbers such as REKN2105.
The recall notice does not specify a remedy, so contact Bard Access Systems, Inc. directly for further instructions.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-2667-2026 — Bard Bard Hello, I own a Bard that is covered by recall Z-2667-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
