Smith & Nephew recalls two surgical products due to mislabeling in shipments. Affected items may be confused with different models, but no safety hazard is reported.
It was reported that a JOURNEY II BCS Femoral OXIN LT SZ5 was in a box labelled as a LEGION NARROW PS OXIN SZ 6N RT.
Smith & Nephew is recalling two surgical products that were mislabeled in shipments. This means some customers might have received the wrong model, but there is no safety risk reported.
The products were mislabeled in shipments, meaning some items were incorrectly labeled as one model when they were actually another. However, the recall does not indicate any safety hazard or injury risk.
Surgical patients and healthcare providers who received the LEGION NARROW PS OXIN SZ 6N RT or JRNY II BCS FEMORAL OXIN LT SZ 5 products. The risk is low as no safety hazard is reported.
Check for the model numbers: 71421276 (LEGION NARROW PS OXIN SZ 6N RT) or 74022125 (JRNY II BCS FEMORAL OXIN LT SZ 5). The products were sold with specific lot numbers and unique identifiers.
Look for the model numbers on the product: 71421276 or 74022125.
No safety hazard is reported in the recall notice.
The recall does not require action as there is no safety risk reported.
Check for model numbers 71421276 or 74022125 on the product labels.
We’ve drafted a message you can send Smith & Nephew to request your refund or repair — edit it as you like.
Subject: Recall Z-1099-2022 — Smith & Nephew Smith & Nephew Hello, I own a Smith & Nephew that is covered by recall Z-1099-2022 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.
