Cardinal Health recalls large surgical gowns with potential sterility compromise due to packaging seal issues. Affected lot numbers and UDI codes listed for verification.
Potential for open packaging seals compromising the sterility of the surgical gowns
Cardinal Health is recalling large surgical gowns that may have packaging seals that don't maintain sterility. This could lead to infections during surgery if the gowns are used without proper sterility.
The packaging seals on these gowns might not hold properly, which could allow contamination. If the gowns are not sterile when used, it could lead to infections during surgery.
Surgical staff and hospitals using Cardinal Health Poly-Reinforced Surgical Gowns Large SKU: 9010 with the listed lot numbers. The risk is highest for those using the gowns in sterile procedures.
Check for lot numbers: 20MDQ014, 21ADQ007, 21CDQ004, 21CDQ005, 21DDQ001, 21DDQ002, 21EDQ001, 21FDQ001, 21GDQ001, 21HDQ001, 21JDQ003. Also look for UDI codes: 50192253018972 (cs) or 10192253018974 (ea).
Verify your gown's lot number and UDI code against the listed numbers to confirm if it's affected.
The recall states there's a potential for open packaging seals compromising sterility, so they should not be used until the issue is resolved.
The recall does not specify a remedy, so you should check the lot numbers and UDI codes to see if your gowns are affected.
Check the lot numbers listed: 20MDQ014, 21ADQ007, 21CDQ004, 21CDQ005, 21DDQ001, 21DDQ002, 21EDQ001, 21FDQ001, 21GDQ001, 21HDQ001, 21JDQ003. Also check UDI codes: 50192253018972 (cs) or 10192253018974 (ea).
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-0372-2022 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-0372-2022 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.
