Smith & Nephew recalls OSTEORAPTOR 2.9 W. 2 UB suture anchors with improper sterile pouch seals that could breach sterility during use. Product numbers and batch dates listed.
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 absorbable suture anchors that may have packaging seals that don't properly protect the sterile product. If the pouch seal is broken, the suture could become contaminated during surgery, risking infection.
The sterile pouch around the suture anchor might not seal properly, allowing bacteria to enter. This could lead to infection if the suture is used during surgery without being properly sterilized.
Surgical patients and medical professionals who use the OSTEORAPTOR 2.9 W. 2 UB suture anchors with the listed product numbers and batch dates. Patients undergoing surgery are most at risk if the suture becomes contaminated.
Check the product number on the packaging: 72201996. Look for batch numbers: 2012912, 2017844, 2019840, 2021496, 2024714, 2033500, 2049663, 2052725, or 2055727. These anchors were sold with specific packaging.
Look for the product number 72201996 and batch numbers listed above on the packaging.
The recall is for packaging that may not seal properly, but the product is safe if the pouch seal is intact. The hazard only occurs if the seal is broken.
The recall does not specify a remedy, so no action is required if the packaging seal appears intact. Check the product number and batch dates to confirm.
The recall does not provide details on how to check the seal. If the pouch appears intact, it is likely safe.
We’ve drafted a message you can send Smith & Nephew to request your refund or repair — edit it as you like.
Subject: Recall Z-0153-2021 — Smith & Nephew Smith & Nephew Hello, I own a Smith & Nephew that is covered by recall Z-0153-2021 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.
