Reported Mar 31, 2021 · Terminated
Femoral Angiography Drape Bulk Non-Sterile
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?
- Femoral Angiography Drape Bulk Non-Sterile
- Lot codes and dates
- Catalog Number 29560NC
- Lot number's
64 of 64 codes
2450ER12660ER12960ER12450ER22660ER22960ER22460ER12670ER12970ER12460ER22670ER22970ER22470ER12690ER13030ER12470ER22690ER23030ER22480ER12720ER13040ER12480ER22720ER23040ER22510ER12730ER13080ER22510ER22730ER23090ER12520ER12740ER13090ER22520ER22740ER23100ER12530ER12750ER13100ER22530ER22750ER23150ER12540ER12760ER13160ER12600ER22760ER23170ER12610ER12820ER13180ER12610ER22820ER23210ER12620ER12830ER13290FR12620ER22830ER23490FR1
- Amount recalled
- 83213 units
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
Why it was recalled
Cardinal Health has determined that a manufacturing variance in a plastic film used to manufacture these products is causing the drapes and leggings to stick , which may prevent the products from being unfolded and applied properly.
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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