Bard Access Systems recalls PowerPICC Provena Catheters (3 Fr. Single lumen and 4 Fr. Dual Lumen) due to possible leaks at the luer hub extension leg junction. Product codes and serial numbers listed in the recall.
Possible leaks on the 3 Fr. Single lumen and 4 Fr. Dual lumen PowerPICC catheters at the luer hub extension leg junction.
Bard Access Systems is recalling PowerPICC Provena Catheters (3 Fr. Single lumen and 4 Fr. Dual Lumen) because they may leak at the luer hub extension leg junction. This could lead to complications for patients using these medical devices.
The catheters may leak at the luer hub extension leg junction, which could cause complications for patients. This is a potential issue with the design of the catheter connections.
Patients using PowerPICC Provena Catheters for medical purposes are likely affected. Those with the specific product codes and serial numbers listed in the recall are most at risk.
Check for product codes and serial numbers listed in the recall, such as S1274108D (REBN2334) or S9274108D (REBN2336). The catheters are packaged in a poly tray with Tyvek lid within a header bag or breather bag configuration.
Look for product codes like S1274108D or S9274108D on the catheter packaging or label.
The catheters may leak at the luer hub extension leg junction, which could cause complications for patients.
Check for product codes such as S1274108D (REBN2334) or S9274108D (REBN2336) on the catheter packaging or label.
The recall does not specify a remedy, so contact Bard Access Systems for further instructions.
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-0536-2018 — Bard Access Systems Bard Access Systems Hello, I own a Bard Access Systems that is covered by recall Z-0536-2018 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.
