Smith & Nephew recalls HEALICOIL RG SA 5.5MM absorbable suture anchors with specific batch numbers due to potential sterile packaging breach. Consumers should check product details and contact Smith & Nephew for guidance.
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 suture anchors because the packaging might not seal properly, risking contamination. This could lead to infection if the product is used without a sterile barrier.
The packaging may not seal correctly, which could breach the sterile barrier. This might allow contamination of the suture anchor, increasing the risk of infection during medical procedures.
Medical professionals and patients who have purchased the recalled HEALICOIL RG SA 5.5MM suture anchors with specific batch numbers. Those using the product for surgery are most at risk.
Check the product number (72203707) and batch numbers listed in the recall notice. The product is an absorbable suture anchor used in surgical procedures.
Identify the product number (72203707) and batch numbers from the list provided in the recall notice.
The recall indicates a potential risk of sterile packaging breach, but the product is not unsafe if the packaging seals properly. Contact Smith & Nephew for specific guidance.
Check the product number and batch numbers listed in the recall notice. If you have the recalled items, contact Smith & Nephew for further instructions.
Look for the product number (72203707) and batch numbers from the list provided in the recall notice.
We’ve drafted a message you can send Smith & Nephew to request your refund or repair — edit it as you like.
Subject: Recall Z-0171-2021 — Smith & Nephew Smith & Nephew Hello, I own a Smith & Nephew that is covered by recall Z-0171-2021 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.
