Smith & Nephew recalls TWINFIX Ultra absorbable suture anchors with potential sterile packaging breaches. Affected units have specific product numbers and batch dates. Consumers should check packaging details to determine if their item is recalled.
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 certain TWINFIX Ultra absorbable suture anchors due to a risk that the sterile packaging could be improperly sealed, potentially allowing contamination. This could lead to infection if the suture is used without proper sterility.
The sterile packaging around the suture anchors may not seal properly, creating a breach that could allow contamination. If the suture is used without a sterile barrier, it might introduce infection during surgery.
Medical professionals who use the suture anchors for surgical procedures are most at risk. Patients who have received the recalled product may also be affected if the packaging was compromised.
Check for Product Number 72202610 and Batch Numbers 2024447 or 2039587 on the packaging. The product is an absorbable suture anchor used in surgical procedures.
Look for Product Number 72202610 and Batch Numbers 2024447 or 2039587 on the packaging.
The recall is for potential packaging issues that could lead to contamination. If the packaging is intact, it may be safe, but the manufacturer recommends checking the specific product details.
Check the packaging for Product Number 72202610 and Batch Numbers 2024447 or 2039587. If you have these details, contact Smith & Nephew for further instructions.
The manufacturer does not specify a stop-use instruction. If the packaging is intact, it may be safe, but the recall indicates a potential risk that requires verification.
We’ve drafted a message you can send Smith & Nephew to request your refund or repair — edit it as you like.
Subject: Recall Z-0158-2021 — Smith & Nephew Smith & Nephew Hello, I own a Smith & Nephew that is covered by recall Z-0158-2021 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.
