Smith & Nephew recalls EVOS Screws with incorrect expiration dates on labels. These screws are used in bone repair procedures. Affected parts include specific model numbers and batch lots.
Multiple or incorrect expiration dates were provided on the affected designation labels.
Smith & Nephew is recalling EVOS Screws that are part of the EVOS MINI plating system for bone repairs. The recall is due to incorrect expiration dates on the product labels, which could lead to using expired screws during medical procedures.
The screws have incorrect expiration dates on their labels. This means the medical team might use expired screws during procedures, which could lead to complications like improper healing or infection.
Medical professionals who use these screws for bone repairs, such as orthopedic surgeons, are most at risk. Patients receiving these screws as part of their treatment may also be affected.
Check if your screws have part numbers like 72424030 or batch lots such as 14FM17199R. These screws are used in bone repair procedures and sold through medical suppliers.
Look for incorrect expiration dates on the screw labels to confirm if they are affected.
The recall is due to multiple or incorrect expiration dates on the affected designation labels, which could lead to using expired screws during medical procedures.
The affected screws have part numbers like 72424030 and batch lots such as 14FM17199R, used in bone repair procedures.
The recall does not require stopping use immediately; however, you should check expiration dates to ensure they are correct.
We’ve drafted a message you can send Smith & Nephew to request your refund or repair — edit it as you like.
Subject: Recall Z-2945-2020 — Smith & Nephew Smith & Nephew Hello, I own a Smith & Nephew that is covered by recall Z-2945-2020 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.
