Stryker recalls certain Femoral Nails (A/R T2 Femur 12x360 mm) due to potential reduced strength causing premature breakage. Affected products have specific product numbers and lot codes.
The manufacturer has discovered that potentially out-of-specification products may have left the factory. Non-conforming cannulation of the nails may result in reduced component strength and potentially premature nail breakage.
Stryker is recalling specific femoral nails that may have weaker strength due to manufacturing issues, which could lead to premature breakage during use. This affects medical devices used in hip surgeries.
The nails may have been produced with specifications that don't meet quality standards. This could cause the nails to break earlier than expected during surgery, potentially leading to complications.
Medical professionals who use these femoral nails for hip surgeries are most at risk. Patients receiving these implants during the recall period could be affected.
Check for the product number 18251236S, lot code K081650, or GTIN 04546540199775 on the device packaging or label.
Look for the product number 18251236S, lot code K081650, or GTIN 04546540199775 on the device packaging or label.
The product number is 18251236S.
The lot code is K081650.
The recall record does not specify a remedy.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2396-2018 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2396-2018 from Stryker. 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.
