Smith & Nephew recalls Ultra Fast-Fix AB Assembly curved absorbable suture anchors with batch numbers 2023195-2054832 due to potential sterile packaging breaches that could compromise surgical safety.
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 specific batches of Ultra Fast-Fix AB Assembly curved absorbable suture anchors because the sterile packaging might not seal properly. This could allow contamination during surgery, making the product unsafe for medical use.
The sterile packaging on these suture anchors may not seal correctly, potentially allowing contaminants to enter the surgical site. This could lead to infections or other complications during surgery if the product is used without proper sterility.
Surgical patients and healthcare providers using the recalled batch numbers of Ultra Fast-Fix AB Assembly curved absorbable suture anchors. Those most at risk are patients undergoing surgery with these specific products.
Check the product's batch number on the packaging, which is listed in the recall as 2023195 through 2054832. The product is a curved absorbable suture anchor used in orthopedic surgeries.
Look for the batch number on the packaging, which should be one of the listed numbers (2023195 to 2054832).
The sterile packaging may not seal properly, which could allow contaminants to enter the surgical site and cause infections or complications during surgery.
Check the batch number on the packaging. If it matches the listed numbers, contact Smith & Nephew for instructions on how to handle the product.
The product is safe for use only if the batch number is not in the recalled list. If you have a recalled batch, do not use it and contact Smith & Nephew for guidance.
We’ve drafted a message you can send Smith & Nephew to request your refund or repair — edit it as you like.
Subject: Recall Z-0144-2021 — Smith & Nephew Smith & Nephew Hello, I own a Smith & Nephew that is covered by recall Z-0144-2021 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.
