Smith & Nephew recalls HEALICOIL RG SA 5.5MM absorbable suture anchors with batch numbers 2013923-2056428 due to potential sterile packaging breaches. Consumers should check product labels for affected batches.
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 RG SA 5.5MM absorbable suture anchors because the sterile packaging might not seal properly. This could allow contamination of the surgical product, posing a risk during medical procedures.
The packaging may not seal correctly, potentially allowing contaminants to enter the sterile product. This could lead to infections or complications during surgery if the suture anchor is used without proper sterility.
Medical professionals and patients who have received the recalled suture anchors during surgery. Those using the product for surgical procedures are most at risk.
Check the product label for batch numbers listed: 2013923 through 2056428. The product is an absorbable suture anchor with the model HEALICOIL RG SA 5.5MM W/2 UB-BL CBR BL.
Look for batch numbers on the label: 2013923 through 2056428.
The recall is for potential packaging issues that could lead to contamination. If the packaging is intact, the product may still be safe, but affected batches should be checked.
Check the batch number on the product label. Affected batches range from 2013923 to 2056428.
The recall does not specify a remedy, so contact Smith & Nephew directly for guidance on handling the 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-0170-2021 — Smith & Nephew Smith & Nephew Hello, I own a Smith & Nephew that is covered by recall Z-0170-2021 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.
