Reported Sep 29, 2021 · Ongoing
Catalog A800361, SureStep" Foley Tray, Bard LubricathTM Foley Catheter Tray
C.R. Bard Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: C.R. Bard Inc · 8195 Industrial Blvd NE · Covington, GA · 30014-1497
Is this the product you have?
- Catalog A800361, SureStep" Foley Tray, Bard LubricathTM Foley Catheter Tray
- Lot codes and dates
7 of 7 products
Products covered by this recall Model / number Barcodes Product as published A80036100801741073939Lots: NGFR0310, UDI (01)00801741073939(17)201220(10) — 00801741073939NGFR0311,UDI N(01)00801741073939(17)201220(10) — 00801741073939GFR2807, UDI (01)00801741073939(17)201220(10) — 00801741073939NGFR2829, UDI (01)00801741073939(17)201220(10) — 00801741073939NGFR3571, UDI (01)00801741073939(17)201220(10) — 00801741073939NGFR5475, UDI (01)00801741073939(17)201220(10) — 00801741073939nd NGFR5481 UDI (01)00801741073939(17)201220(10) - Amount recalled
- 33,380 units
This recall covers 21 products
The agency filed one notice per product. You are reading one of them; the other 20 are below.
8 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
There is potential for packaging defects that may impact the sterile barrier.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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