Smith & Nephew recalls OSTEORAPTOR 2.3 absorbable suture anchors with batch numbers 2012908-2056870 due to potential sterile pouch breaches. Affected users should check product packaging for batch numbers.
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 absorbable suture anchors with specific batch numbers because the sterile packaging might not seal properly, risking contamination. This could lead to infections if the suture is used without a clean seal.
The sterile pouch surrounding the suture anchor may not seal correctly, allowing contaminants to enter. This could lead to infections if the anchor is used without a properly sealed pouch.
Orthopedic surgeons and medical professionals who use the OSTEORAPTOR 2.3 suture anchors with batch numbers listed in the recall. Patients receiving these anchors during surgery are at risk if the packaging is compromised.
Check the product packaging for batch numbers: 2012908, 2016123, 2017811, 2018793, 2018796, 2019889, 2023270, 2024438, 2025338, 2027482, 2029362, 2032556, 2033493, 2034379, 2034380, 2034381, 2036272, 2036273, 2038763, 2050882, 2050883, 2049650, 2049651, 2053757, 2056870.
Look for batch numbers on the packaging to determine if your item is affected.
The sterile pouch surrounding the suture anchor may not seal properly, potentially allowing contaminants to enter.
Check the product packaging for batch numbers listed in the recall. If your batch number matches, contact Smith & Nephew for further instructions.
The recall addresses potential contamination risks, but the product itself does not pose a direct risk of serious injury in normal use.
We’ve drafted a message you can send Smith & Nephew to request your refund or repair — edit it as you like.
Subject: Recall Z-0149-2021 — Smith & Nephew Smith & Nephew Hello, I own a Smith & Nephew that is covered by recall Z-0149-2021 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.
