Cardinal Health recalls SmartGown Breathable Surgical Gowns with raglan sleeves X-large, X-long, A-line SKU 32474 due to potential open packaging seals compromising sterility. Affected units include specific lot numbers and UDI codes.
Potential for open packaging seals compromising the sterility of the surgical gowns
Cardinal Health is recalling SmartGown Breathable Surgical Gowns with raglan sleeves X-large, X-long, and A-line models (SKU 32474) because the packaging seals might not stay closed, risking contamination during surgery. This could lead to infections if the gowns are used without proper sterility.
The packaging seals on these surgical gowns may not stay closed properly, which could allow contamination. If the gowns are not sterile when used during surgery, it might lead to infections for patients or staff.
Surgical staff and hospitals that purchased the specific lot numbers and UDI codes listed for SmartGown gowns. The risk is highest for those using the gowns in sterile environments where contamination could occur.
Check for the SKU number 32474 on the gown label. Look for lot numbers starting with 20MFQ or 21AFQ through 21JFQ, and UDI codes 50192253018927 (Cs) or 10192253018929 (Ea).
Inspect the packaging seal for any signs of being open or damaged before use.
The recall indicates a potential risk to sterility, so they should not be used until the packaging seal is confirmed closed.
The recall does not specify a return or replacement process; check the packaging seal before use.
Look for the SKU 32474, lot numbers starting with 20MFQ or 21AFQ through 21JFQ, and UDI codes 50192253018927 (Cs) or 10192253018929 (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-0368-2022 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-0368-2022 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.
