Cardinal Health 200, LLC Nonsterile Radial/Femoral Angiography Drape, Catalog Number 29529N - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Nonsterile Radial/Femoral Angiography Drape, Catalog Number 29529N - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.
Brand
Cardinal Health 200, LLC
Lot Codes / Batch Numbers
Lot Numbers: 2320DR1, 2330DR1, 2410DR1, 2440DR1, 2450DR1, 2580DR1, 2670DR1, 2730DR1, 2740DR1, 2790DR1, 2830DR1, 2860DR1, 2870DR1, 2890DR1, 2900DR1, 2930DR1, 2940DR1, 2950DR1, 3080DR1, 3310DR1, 3320DR1, 3330DR1, 3350DR1
Products Sold
Lot Numbers: 2320DR1, 2330DR1, 2410DR1, 2440DR1, 2450DR1, 2580DR1, 2670DR1, 2730DR1, 2740DR1, 2790DR1, 2830DR1, 2860DR1, 2870DR1, 2890DR1, 2900DR1, 2930DR1, 2940DR1, 2950DR1, 3080DR1, 3310DR1, 3320DR1, 3330DR1, 3350DR1
Cardinal Health 200, LLC is recalling Nonsterile Radial/Femoral Angiography Drape, Catalog Number 29529N - Product Usage: intended to be u due to The plastic film used to manufacture these Angiography Drape and Cesarean Birth Drape products is causing the drapes to stick, which may prevent the p. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
The firm initiated the recall by letter on 05/20/2021. The letter explained the issue and the hazard, and requested the return of the units.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026