C.R. Bard recalls 14Fr SURESTEP intermittent catheter trays with potential leak at catheter-drain bag connection. Affected units have specific serial numbers. Contact for remedy.
There is a potential to leak from the catheter where it connects to the drain bag
C.R. Bard is recalling intermittent catheter trays that may leak at the connection point to the drain bag. This could lead to infections or discomfort for users. The recall affects specific model numbers with unique serial codes.
The catheter may leak at the connection to the drain bag, potentially causing infections or discomfort. This leak risk occurs during normal use but is not immediately dangerous.
Patients using intermittent catheter systems are most at risk. This recall applies to specific model numbers sold with unique serial codes.
Check for the model number 14Fr SURESTEP INTERMITTENT CATHETER TRAY with serial numbers starting with NGEWX117 or similar codes listed in the recall notice.
Look for serial numbers starting with NGEWX117, NGEEX133, NGEY0842, or NGEZ1823 followed by specific codes.
The recall is due to a potential leak at the catheter connection to the drain bag, which could cause infections or discomfort.
Check for the model number 14Fr SURESTEP INTERMITTENT CATHETER TRAY with serial numbers starting with NGEWX117, NGEEX133, NGEY0842, or NGEZ1823 followed by specific codes.
The recall does not specify a remedy, so contact C.R. Bard for further instructions.
We’ve drafted a message you can send C.R. Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-0667-2022 — C.R. Bard C.R. Bard Hello, I own a C.R. Bard that is covered by recall Z-0667-2022 from C.R. 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.
