C.R. Bard recalls SureStep Foley Trays with potential packaging defects that could compromise sterile barriers. Affected units include specific catalog numbers and lots. Consumers should check their product details to determine if they are impacted.
There is potential for packaging defects that may impact the sterile barrier.
C.R. Bard is recalling SureStep Foley Trays due to potential packaging defects that might compromise the sterile barrier. This could lead to infection risks during medical procedures if the device is not properly sterilized.
The packaging defects could allow contamination to reach the sterile barrier of the Foley tray. This might compromise the device's sterility during medical procedures, increasing infection risks for patients.
Patients using medical catheters or urinary drainage systems who own the specific catalog number A897514 and lot NGFR2808 are most at risk. Healthcare providers using these devices in medical settings may also be affected.
Check for catalog number A897514 and lot number NGFR2808 on the packaging. The device is sold as a silicone drainage bag with StatLock stabilization.
Identify the catalog number and lot number on the packaging to confirm if your device is affected.
This recall specifically affects SureStep Foley Trays with catalog number A897514 and lot NGFR2808. If your device matches these details, it is affected.
The recall does not include a remedy, so you should check your product details to determine if it is affected. If it is, contact C.R. Bard for further instructions.
Look for catalog number A897514 and lot number NGFR2808 on the packaging. The device is a silicone drainage bag with StatLock stabilization.
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-2533-2021 — C.R. Bard C.R. Bard Hello, I own a C.R. Bard that is covered by recall Z-2533-2021 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.
