Cardinal Health recalls sterile femoral angiography drapes with catalog numbers 29460 and 29456 due to plastic film causing sticking that may prevent proper unfolding. Affected items include specific lot numbers.
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 with catalog numbers 29460 and 29456 because the plastic film causes them to stick, making it 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, which prevents the drapes from being unfolded and applied 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 receiving these drapes during medical treatments may be affected if the drapes don't apply correctly.
Check for catalog numbers 29460 or 29456. Look for specific lot numbers: 20LRS055, 20MRS073, 21ARS042 for 29460 and 20MMR062 for 29456.
Identify the catalog number and lot number to confirm if your drape is affected.
The plastic film causes the drapes to stick, which may prevent proper unfolding and application during medical procedures.
Catalog numbers 29460 and 29456.
For catalog 29460: lot numbers 20LRS055, 20MRS073, 21ARS042; for catalog 29456: lot number 20MMR062.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-2037-2021 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-2037-2021 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.
