Smith & Nephew recalls HEALICOIL RSB SA 5.5MM absorbable suture anchors with batch numbers 2014002 to 2057402 due to potential sterile packaging breaches. Affected users should check their product numbers and contact the company for details.
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 5.5MM absorbable suture anchors because the sterile packaging might not seal properly, risking contamination. This could lead to infections if the suture is used without proper sterility.
The packaging may not seal correctly, which could allow contaminants to enter the sterile product. This might lead to infections if the suture is used without proper sterility during medical procedures.
Surgical patients and medical professionals who own or use the recalled HEALICOIL RSB SA 5.5MM suture anchors with specific batch numbers. Those undergoing surgery or procedures using these anchors are most at risk.
Check the product number on the packaging, which is listed as 72203708. The affected batch numbers range from 2014002 to 2057402. The product is an absorbable suture anchor used in surgical procedures.
Look for the product number 72203708 on the packaging to confirm if it's affected.
Check if your batch number falls within the range 2014002 to 2057402.
The product number is 72203708.
Batch numbers from 2014002 to 2057402 are affected.
Check the product number on the packaging (72203708) and verify if your batch number is in the range 2014002 to 2057402.
We’ve drafted a message you can send Smith & Nephew to request your refund or repair — edit it as you like.
Subject: Recall Z-0172-2021 — Smith & Nephew Smith & Nephew Hello, I own a Smith & Nephew that is covered by recall Z-0172-2021 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.
