Bard Access Systems recalls PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen with UDI-DI Code 00801741129674 due to lidocaine ampoules manufactured under deficient practices. Affected units may pose risks from improper manufacturing.
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 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen models with UDI-DI Code 00801741129674 because lidocaine ampoules used in their production were made under deficient manufacturing practices. This recall is important because improper manufacturing could lead to potential risks with the catheter's use.
The recall is due to lidocaine ampoules being produced under deficient manufacturing practices by the supplier. This could potentially lead to issues with the catheter's safety and effectiveness during medical procedures.
Healthcare professionals using Bard PowerPICC SOLO HF Catheters with the specific UDI-DI Code 00801741129674 are most at risk due to the lidocaine ampoules being manufactured under deficient practices.
Check for the UDI-DI Code 00801741129674 on the catheter packaging or label. The affected model is PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen with lot number REKT1554.
Identify the UDI-DI Code 00801741129674 and lot number REKT1554 on the catheter packaging or label.
The lidocaine ampoules used in manufacturing were produced under deficient practices by the supplier, which could pose risks.
Check for the UDI-DI Code 00801741129674 and lot number REKT1554 on the catheter packaging or label.
The official recall notice does not specify a remedy or action steps beyond checking product details.
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-2658-2026 — Bard Access Systems Bard Access Systems Hello, I own a Bard Access Systems that is covered by recall Z-2658-2026 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.
