C.R. Bard recalls SureStep Foley Trays with potential packaging defects that could compromise sterile barrier. Affected units include specific lots and expiration dates. Consumers should check product details and contact Bard for guidance.
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 break the sterile barrier. This could lead to infections if the device is used without proper sterility. The recall affects specific lots with known expiration dates.
Packaging defects could compromise the sterile barrier of the Foley tray, increasing the risk of infection if the device is used without proper sterility. This is a potential issue for medical devices that require aseptic conditions.
Healthcare professionals and patients using the SureStep Foley Trays with specific lot numbers and expiration dates. Those using the product for medical purposes are most at risk.
Check for lot numbers NGEVX103 (exp. 08/31/2022), NGFR3290 (exp. 02/28/2023), NGFR3291 (exp. 02/28/2023), or NGFR4542 (exp. 02/28/2023) on the packaging. The product is part of the SureStep Foley Tray line from C.R. Bard.
Look for lot numbers NGEVX103 (exp. 08/31/2022), NGFR3290, NGFR3291, or NGFR4542 (exp. 02/28/2023) on the packaging.
The SureStep Foley Tray with lot numbers NGEVX103 (exp. 08/31/2022), NGFR3290, NGFR3291, or NGFR4542 (exp. 02/28/2023).
There is potential for packaging defects that may impact the sterile barrier, increasing infection risk.
Check the product details to see if it is affected. Contact C.R. Bard for further guidance.
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-2525-2021 — C.R. Bard C.R. Bard Hello, I own a C.R. Bard that is covered by recall Z-2525-2021 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.
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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.
