Smith & Nephew recalls specific femoral head implants due to incorrect size packaging. This may lead to improper fit during surgery. Affected units include REF 71343204 (32mm) and REF 71343604 (36mm) with batch numbers.
Packaging contained the incorrect size of femoral head from what was displayed on the label.
Smith & Nephew is recalling certain femoral head implants because the packaging listed the wrong size. This could cause improper fitting during surgery if used incorrectly. The recall affects specific batch numbers and model sizes.
The packaging contains the incorrect size of the femoral head compared to what's labeled. This could lead to improper fitting during surgery if the wrong size is used. However, the error is in the packaging, not the product itself.
Orthopedic surgeons and medical professionals who use these implants for joint replacements. Patients receiving these implants are not directly affected by the packaging error.
Check for the product code REF 71343204 (32mm) or REF 71343604 (36mm) with batch numbers 23FM03219 or 23FM04184. These implants were sold with specific expiration dates of June 2033.
Verify the product code and batch number on the packaging to confirm if it's affected.
The recall specifies that the packaging listed the incorrect size. The correct sizes are 32mm and 36mm as per the product codes.
No, the recall does not require stopping use. The issue is with packaging labeling, not the product itself.
Check for the product codes REF 71343204 (32mm) or REF 71343604 (36mm) with batch numbers 23FM03219 or 23FM04184.
We’ve drafted a message you can send Smith & Nephew to request your refund or repair — edit it as you like.
Subject: Recall Z-1901-2024 — Smith & Nephew Smith & Nephew Hello, I own a Smith & Nephew that is covered by recall Z-1901-2024 from Smith & Nephew. 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.
