Reported Jul 14, 2021 · Terminated
Nonsterile Femoral Angiography Drape, Catalog Numbers: a) 29460NB, b) 29456NB - Product Usage: intended to be used as…
Cardinal Health 200, LLC
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: Cardinal Health 200, LLC · 3651 Birchwood Dr · Waukegan, IL · 60085-8337
Is this the product you have?
- Nonsterile Femoral Angiography Drape
- Catalog Numbersa) 29460NB
- b) 29456NB - Product Usageintended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination
- Lot codes and dates
- a) 29460NBLot
- Numbers
0071PR10121PR10131PR10141PR10271PR10281PR10291PR10351PR10361PR10391PR10401PR13040PR13110PR13250PR13380PR13510PR13520PR13530PR1
- b) 29456NBLot
- Numbers
3290LR13300LR13310LR13320LR13350LR13390LR13420LR1
- Amount recalled
- 15360 units
This recall covers 8 products
The agency filed one notice per product. You are reading one of them; the other 7 are below.
Where it was sold
- Nationwide
Why it was recalled
The plastic film used to manufacture these Angiography Drape and Cesarean Birth Drape products is causing the drapes to stick, which may prevent the products from being unfolded and applied properly. Sold in single sterile and bulk non-sterile configurations.
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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