Smith & Nephew recalls OSTEORAPTOR 2.3 W 1UB II Blue Absorbable Suture anchors with incomplete sterile packaging that could breach the sterile barrier.
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 OSTEORAPTOR 2.3 W 1UB II Blue Absorbable Suture anchors due to potential packaging issues that might compromise the sterile barrier. This could lead to infection or contamination during medical procedures if the product is used without a properly sealed pouch.
The packaging may not seal properly, which could breach the sterile barrier around the suture anchor. This might allow contamination or infection during surgery if the product is used without a fully intact sterile pouch.
Patients who received this specific suture anchor product from Smith & Nephew. Surgeons and medical staff using the product are most at risk if the sterile barrier is compromised.
Check for the product number 72201991 and batch numbers listed in the recall notice (e.g., 2012767, 2013997, 2016120). The product is a blue absorbable suture anchor used in surgical procedures.
Verify the product number and batch numbers listed in the recall notice to confirm if your item is affected.
The recall indicates potential packaging issues that could compromise sterility, but the product is safe if the packaging seals properly. Affected units should be checked as per the recall instructions.
The recall does not specify a remedy, so check the product details against the listed batch numbers to determine if it's affected. Contact Smith & Nephew for further guidance.
Look for the product number 72201991 and batch numbers from the list provided in the recall notice (e.g., 2012767, 2013997).
We’ve drafted a message you can send Smith & Nephew to request your refund or repair — edit it as you like.
Subject: Recall Z-0148-2021 — Smith & Nephew Smith & Nephew Hello, I own a Smith & Nephew that is covered by recall Z-0148-2021 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.
