Cardinal Health recalls sterile femoral angiography drapes with catalog number 29525 due to plastic film causing sticking, which may prevent proper unfolding and application. Affected lot numbers: 20LJS033, 20MJS072.
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.
Cardinal Health is recalling sterile femoral angiography drapes that stick due to plastic film, making them hard to unfold and apply properly. This could lead to improper use during medical procedures.
The plastic film in the drapes causes them to stick together, making it difficult to unfold and apply them properly. This could lead to improper isolation of surgical sites from contamination during medical procedures.
Healthcare professionals using these drapes for surgical procedures are most at risk. Patients undergoing procedures with these drapes could be affected if the drapes don't apply correctly.
Check for the catalog number 29525 on the drape packaging. Affected lot numbers are 20LJS033 and 20MJS072. These drapes are sold as single sterile and bulk non-sterile configurations.
Look for lot numbers 20LJS033 or 20MJS072 on the drape packaging.
The plastic film used in these drapes causes them to stick, which may prevent proper unfolding and application during medical procedures.
Check the lot number on the packaging. If it's 20LJS033 or 20MJS072, contact Cardinal Health for instructions.
Yes, if the drape sticks and can't be unfolded properly, it may lead to improper isolation of surgical sites from contamination.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-2031-2021 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-2031-2021 from Cardinal Health. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
