Nonsterile Femoral Angiography Drape recall: Sterility Concern
Nonsterile Femoral Angiography Drape, Catalog Numbers: a) 29460NB, b) 29456NB - Product Usage: intended to be used as protective patient coverings…
Why was Nonsterile Femoral Angiography Drape 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
a) 29460NB: Lot Numbers: 0071PR1, 0121PR1, 0131PR1, 0141PR1, 0271PR1, 0281PR1, 0291PR1, 0351PR1, 0361PR1, 0391PR1, 0401PR1, 3040PR1, 3110PR1, 3250PR1, 3380PR1, 3510PR1, 3520PR1, 3530PR1 b) 29456NB: Lot Numbers: 3290LR1, 3300LR1, 3310LR1, 3320LR1, 3350LR1, 3390LR1, 3420LR1
- Product
- Nonsterile Femoral Angiography Drape, Catalog Numbers: a) 29460NB, b) 29456NB - Product Usage: intended to be used as protective patient coverings…
- Recalling firm
- Cardinal Health 200, LLC
- Quantity
- 15360 units
- Distribution
- US Nationwide distribution.
- Recall date
- July 14, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)