Smith & Nephew recalls specific stem sizes due to incorrect label indicating size 1 instead of -1. This may cause confusion in medical use. Affected items have unique reference numbers.
Complaints were received indicating that the outer label incorrectly identified the product as size "1" instead of "-1". The product contained within the package is size "-1"
Smith & Nephew is recalling certain stem sizes because the product label incorrectly states size "1" instead of "-1". This labeling error could lead to incorrect use in medical procedures, though the product itself is safe.
The product label incorrectly identifies the size as "1" instead of "-1". This labeling error could lead to using the wrong size in medical procedures, potentially causing complications. However, the product itself is safe and the hazard is purely informational.
Medical professionals and patients using the specific stem sizes listed in the recall. Those most at risk are individuals who rely on precise size identification for surgical procedures.
Check for the reference numbers listed: 11CM01091T, 11EM12764T, 11EM12764U, 13MM16036B, 14GM13037D, 15MM09360A, 15MM10833A, 18CM24036, and 18EM15257. The product is labeled as size "-1" but the outer label incorrectly says size "1".
Look for the reference numbers listed in the recall to confirm if your item is affected.
The product label incorrectly states size "1" instead of "-1". This labeling error could lead to incorrect use in medical procedures.
No, the product itself is safe. The hazard is purely a labeling error that could cause confusion in medical use.
Check the reference numbers listed in the recall to see if your item is affected. If it is, you may need to verify the correct size for your procedure.
We’ve drafted a message you can send Smith & Nephew to request your refund or repair — edit it as you like.
Subject: Recall Z-1029-2019 — Smith & Nephew Smith & Nephew Hello, I own a Smith & Nephew that is covered by recall Z-1029-2019 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.
