Bard Access Systems recalls specific Power-Trialysis dialysis catheters due to lidocaine ampoules manufactured under deficient practices. Affected units have UDI-DI codes and lot numbers listed. Consumers should check their catheter details and contact Bard for guidance.
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 certain Power-Trialysis short-term dialysis catheters because lidocaine ampoules used in their production were made under deficient manufacturing practices. This recall affects patients using these catheters for hemodialysis or similar treatments.
The recall is due to lidocaine ampoules being manufactured under deficient practices by the supplier. This could lead to potential issues with the catheter's safety and effectiveness during medical procedures, though the exact risk is not clearly specified in the notice.
Patients using the recalled Power-Trialysis dialysis catheters for hemodialysis or apheresis treatments are most at risk. The recall applies to specific model numbers and lot numbers listed in the notice.
Check for the UDI-DI code (00801741086953, 00801741086977, 00801741086984, 00801741075087, 00801741075100, 00801741066054) and lot numbers (REKX1755, REKW0663, REKY2472, REKZ0393, REKQ1130, REKX3745, REKY2418, REKY2420) on the catheter packaging.
Look for the UDI-DI code and lot number on the catheter packaging to confirm if it is affected.
The recall is due to lidocaine ampoules being manufactured under deficient practices by the supplier, which could affect the catheter's safety and effectiveness.
The affected models include Power-Trialysis Short-Term Straight Dialysis Catheter (13 Fr Triple-Lumen) with UDI-DI codes 00801741086953, 00801741086977, 00801741086984, and Power-Trialysis Short-Term Curved Extension Dialysis Catheter (13 Fr Triple-Lumen) with UDI-DI code 00801741075087, 00801741075100, and Power-Trialysis Short-Term Alphacurve Dialysis Catheter (13 Fr Triple-Lumen) with UDI-DI code 00801741066054.
The recall notice does not specify a remedy, so contact Bard Access Systems directly for guidance on next steps.
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-2660-2026 — Bard Access Systems Bard Access Systems Hello, I own a Bard Access Systems that is covered by recall Z-2660-2026 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.
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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.
