Cardinal Health recalls sterile femoral angiography drapes due to manufacturing variance causing sticking. This may prevent proper application. Check catalog numbers 29560 and lot numbers 20LQR067/20MQR023.
Cardinal Health has determined that a manufacturing variance in a plastic film used to manufacture these products is causing the drapes and leggings to stick , which may prevent the products from being unfolded and applied properly.
Cardinal Health is recalling sterile femoral angiography drapes that may stick together due to a manufacturing issue. This could prevent proper application during medical procedures. Affected items have specific catalog and lot numbers.
The drapes may stick together due to a manufacturing variance in the plastic film. This sticking could prevent the drapes from being unfolded and applied correctly during medical procedures.
Healthcare professionals using these drapes for medical procedures are most likely affected. Patients receiving procedures using the recalled drapes could be at risk if the drapes don't apply properly.
Check for catalog number 29560 on the drape packaging. Lot numbers 20LQR067 (expiring November 2025) and 20MQR023 (expiring December 2025) are also affected.
Look for catalog number 29560 and lot numbers 20LQR067 or 20MQR023 on the drape packaging.
Cardinal Health determined that a manufacturing variance in the plastic film causes the drapes to stick together, which may prevent proper application during medical procedures.
The recall record does not specify a remedy, so check with Cardinal Health directly for instructions.
The drapes may stick together, potentially preventing proper application during medical procedures. This could lead to complications if not handled correctly.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-1303-2021 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-1303-2021 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.
