Smith & Nephew recalls TWINFIX 6.5mm absorbable suture anchors with potential sterile packaging breach. Product number 7210713, batch 2027380. Affected users should check packaging for seal integrity.
Product packaging improper or incomplete seal of the pouch surrounding the sterile product may result in a breach of the sterile barrier created by the pouch
Smith & Nephew is recalling TWINFIX 6.5mm absorbable suture anchors due to possible packaging breaches that could compromise sterility. This could lead to infections if the product is used without a sterile barrier.
The sterile pouch packaging may not seal properly, allowing contamination. If the pouch breaches, the suture anchors could become non-sterile, increasing infection risk during surgery.
Medical professionals and surgical teams using the TWINFIX 6.5mm absorbable suture anchors with product number 7210713 and batch 2027380. The risk is lowest for users who verify packaging integrity before use.
Check for product number 7210713 and batch number 2027380 on the packaging. The TWINFIX 6.5mm absorbable suture anchors are sold by Smith & Nephew.
Inspect the pouch for any signs of improper sealing before use.
The product may have a packaging breach that could compromise sterility. Users should check the seal before use.
Check the packaging for product number 7210713 and batch number 2027380. If the pouch seal appears intact, it may be safe to use.
Look for product number 7210713 and batch number 2027380 on the packaging. The TWINFIX 6.5mm absorbable suture anchors are the affected product.
We’ve drafted a message you can send Smith & Nephew to request your refund or repair — edit it as you like.
Subject: Recall Z-0140-2021 — Smith & Nephew Smith & Nephew Hello, I own a Smith & Nephew that is covered by recall Z-0140-2021 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.
