Bard recalls SureStep Foley Trays with potential packaging defects that could compromise sterile barrier. Affected units include specific catalog numbers and lots. Consumers should contact Bard for details.
There is potential for packaging defects that may impact the sterile barrier.
Bard is recalling SureStep Foley Trays that may have packaging defects risking sterile barrier failure. This could lead to infection if the tray is used improperly. Affected units have specific catalog numbers and lots listed in the recall.
Packaging defects might compromise the sterile barrier, potentially allowing contamination. This could increase infection risk during medical procedures if the tray is not properly sterilized.
Healthcare professionals and patients using Bard SureStep Foley Trays with the listed catalog numbers and lots are affected. Those handling the trays during medical procedures are at higher risk.
Check for catalog number A800361 and specific lots listed: NGFR0310, NGFR0311, GFR2807, NGFR2829, NGFR3571, NGFR5475, NGFR5481. The units were sold with UDI codes starting with (01)00801741073939(17)201220(10).
Identify the catalog number and lot numbers listed in the recall notice to confirm if your unit is affected.
The recall is due to potential packaging defects that may impact the sterile barrier, increasing infection risk during medical procedures.
Check for catalog number A800361 and specific lots: NGFR0310, NGFR0311, GFR2807, NGFR2829, NGFR3571, NGFR5475, NGFR5481. The units have UDI codes starting with (01)00801741073939(17)201220(10).
The recall notice does not specify a remedy, so contact Bard directly for further instructions.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-2531-2021 — Bard Bard Hello, I own a Bard that is covered by recall Z-2531-2021 from 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.
