Smith & Nephew recalls HEALICOIL RSB SA 4.75MM absorbable suture anchors with specific batch numbers due to potential sterile packaging breach. Affected products may not stay sterile, risking infection during surgery.
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 HEALICOIL RSB SA 4.75MM absorbable suture anchors because the packaging might not seal properly, which could lead to contamination during surgery. This is serious for surgical procedures where sterility is critical.
The packaging around the sterile suture anchors might not seal correctly, allowing contaminants to enter. This could cause infections during surgery if the product is not properly sterile when used.
Surgical patients and medical professionals who used the recalled suture anchors. Those with the specific batch numbers listed are most at risk of infection if the packaging breaches during surgery.
Check the product number on the packaging (72203704) and batch numbers listed in the recall (e.g., 2014657, 2013922, etc.). The product is an absorbable suture anchor sold for surgical use.
Look for the product number 72203704 and batch numbers listed in the recall (e.g., 2014657, 2013922, etc.) on the packaging.
The packaging may not seal properly, which could breach the sterile barrier and lead to contamination during surgery.
Check the product number and batch numbers listed in the recall. If you have the recalled items, contact Smith & Nephew for guidance.
Yes, if the packaging breaches during surgery, it could lead to infection due to contamination.
We’ve drafted a message you can send Smith & Nephew to request your refund or repair — edit it as you like.
Subject: Recall Z-0168-2021 — Smith & Nephew Smith & Nephew Hello, I own a Smith & Nephew that is covered by recall Z-0168-2021 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.
