Cardinal Health recalls sterile cesarean birth drapes with dual layer anesthesia screen (catalog 29442) due to plastic film causing sticking. This may prevent proper unfolding and application. Affected lot numbers: 20LRR092, 20MRR079.
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 cesarean birth drapes that may stick due to plastic film, preventing proper unfolding and application. This could lead to improper surgical site isolation during childbirth.
The plastic film in the drapes causes them to stick together, making it difficult to unfold and apply correctly. This could lead to improper isolation of the surgical site from contamination during childbirth.
Healthcare providers using these drapes for cesarean sections during childbirth. The risk is highest for medical staff handling the drapes in surgical settings.
Look for the product name 'Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen' with catalog number 29442. Affected lot numbers are 20LRR092 and 20MRR079.
Identify the lot number on the drape packaging to see if it's 20LRR092 or 20MRR079.
The plastic film used in these drapes causes them to stick, which may prevent proper unfolding and application during childbirth.
The recall record does not specify a remedy, so no action is required beyond checking the lot number.
The recall record does not mention patient risks, only that improper use could affect surgical site isolation.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-2035-2021 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-2035-2021 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.
