Bard Access Systems recalls two soft tissue biopsy trays due to lidocaine ampoules being manufactured under deficient practices. These trays may pose a risk if used with affected ampoules.
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Bard Access Systems is recalling two models of soft tissue biopsy trays because the lidocaine ampoules they come with were made using poor manufacturing practices. This could lead to issues if the trays are used with these ampoules.
The lidocaine ampoules in the recalled trays were manufactured under deficient practices, which could lead to improper handling or use. This might cause issues during medical procedures if the ampoules are used as intended.
Healthcare professionals who use these biopsy trays with lidocaine ampoules from the recalled lots are affected. Patients receiving procedures using these trays may be at risk.
Check for the UDI-DI codes 0110885403108563 or 0110885403108501 on the trays. The lot numbers REKY3390 or REKY3393, REJZ0942, REJZ0943 are also associated with the recalled items.
Identify the UDI-DI code and lot number on the tray to confirm if it is recalled.
The lidocaine ampoules in these trays were manufactured under deficient practices by the supplier, which could lead to improper use.
Check the UDI-DI code and lot number on the tray to see if it is part of the recall. If it matches the recalled codes, contact Bard Access Systems for further instructions.
The recall is due to manufacturing deficiencies in the lidocaine ampoules, but the specific safety risks are not clearly described in the official notice.
We’ve drafted a message you can send Bard Access Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-2668-2026 — Bard Access Systems Bard Access Systems Hello, I own a Bard Access Systems that is covered by recall Z-2668-2026 from Bard Access Systems. 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.
