Reported Jul 14, 2021 · Terminated
Nonsterile Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen, Catalog Number 29442N - Product Usage:…
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 Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen
- Catalog Number 29442N - 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
- Lot Numbers
0121QR20391RR13070QR13280QR13280QR23290QR13290QR23300QR13300QR23310QR13310QR23320QR13570QR13570QR2
- Lot Numbers
- Amount recalled
- 6461 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.
Want the full recall guide?
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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