Bard recalls specific poly midline catheters due to lidocaine ampoules made under deficient manufacturing practices. Affected units have UDI-DI codes 00801741121609 and 00801741108051. Contact Bard for details.
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Bard is recalling certain poly midline catheters because lidocaine ampoules used in their production were made under deficient manufacturing practices. This recall affects patients receiving intravenous treatments who use these catheters.
Lidocaine ampoules manufactured under deficient practices could lead to medication errors or improper dosing. This risk is specific to the recalled catheter models and their associated ampoules.
Patients using Bard's poly midline catheters for intravenous treatments are affected. Healthcare providers administering these catheters are most at risk due to potential medication errors.
Check for UDI-DI codes 00801741121609 or 00801741108051 on the catheter packaging. The affected models include CK000495A and CK000566 poly midline catheters.
Identify the UDI-DI code on the catheter packaging to confirm if it is one of the recalled codes: 00801741121609 or 00801741108051.
The recall is due to lidocaine ampoules being manufactured under deficient practices by the supplier, which could lead to medication errors.
The official recall notice does not specify a remedy or action for affected users.
Yes, the affected models are CK000495A and CK000566 poly midline catheters with UDI-DI codes 00801741121609 and 00801741108051.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-2656-2026 — Bard Bard Hello, I own a Bard that is covered by recall Z-2656-2026 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.
