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 and contact the company for guidance.
There is potential for packaging defects that may impact the sterile barrier.
C.R. Bard is recalling SureStep Foley Trays with packaging defects that might break the sterile barrier. This could lead to infections if the device isn't properly sealed during medical use.
Packaging defects could compromise the sterile barrier, allowing contaminants to enter the device. This might lead to infections if the device is used without proper sterilization during medical procedures.
Healthcare professionals using the SureStep Foley Trays for medical procedures are most at risk. Patients receiving these devices during surgery or hospital stays may also be affected if the sterile barrier fails.
Check for the catalog number A899916 on the product. Affected lots include NGFR0101 with UDI (01)00801741074011(17)251228(10).
Look for the catalog number A899916 and the specific lot number NGFR0101 with UDI (01)00801741074011(17)251228(10) on the packaging.
The recall addresses potential packaging defects that could compromise the sterile barrier, but the risk of infection is low if the device is used properly.
Check for the catalog number A899916 and the specific lot number NGFR0101 with UDI (01)00801741074011(17)251228(10) on the product packaging.
The recall does not specify a remedy, so contact C.R. Bard directly for guidance on next steps.
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-2534-2021 — C.R. Bard C.R. Bard Hello, I own a C.R. Bard that is covered by recall Z-2534-2021 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.
