C.R. Bard recalls SureStep Foley Trays with potential packaging defects that could compromise sterile barrier. 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, Urine Meters, and Stabilization Devices due to potential packaging defects that might affect the sterile barrier. This could lead to contamination risks during medical procedures.
The packaging defects could compromise the sterile barrier of the medical devices, potentially leading to contamination during use. This risk is specific to the affected units and does not pose an immediate danger in normal use.
Healthcare professionals and patients using the SureStep Foley Trays, Urine Meters, or StatLock Stabilization Devices are likely affected. Those with the specific catalog numbers and lots listed in the recall are at risk.
Check for the catalog number A902916 and specific lots: NGFR3115, NGFR3278, NGFR3279, NGFS1308, NGFS1309, or NGFS1366. The devices were sold with a unique identifier (UDI) starting with (01)00801741074073.
Identify if your SureStep Foley Tray, Urine Meter, or StatLock Stabilization Device matches the catalog numbers and lots listed in the recall.
The recall states there is potential for packaging defects that may impact the sterile barrier of the devices.
Check for the catalog number A902916 and specific lots: NGFR3115, NGFR3278, NGFR3279, NGFS1308, NGFS1309, or NGFS1366.
The recall does not specify a stop-use action; the hazard is low risk and does not require immediate discontinuation.
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-2536-2021 — C.R. Bard C.R. Bard Hello, I own a C.R. Bard that is covered by recall Z-2536-2021 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.
