Stryker recalls specific femoral nails due to potential reduced strength from manufacturing issues, which could cause premature breakage during use.
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 certain femoral nails that may have weaker strength due to manufacturing defects. This could lead to the nails breaking prematurely during surgery, potentially causing complications for patients.
The recalled femoral nails may have been produced with specifications that don't meet quality standards. This could result in the nails becoming weaker than expected, increasing the risk of breaking during surgical procedures.
Surgical teams using the recalled femoral nails for orthopedic procedures are most at risk. Patients undergoing surgery with these specific nails may experience complications if the nails break unexpectedly.
Check for the product number 18511446S on the nail packaging. The lot code K0748D3 and GTIN 07613252129295 are also associated with this recall.
Verify the product number on the nail packaging to confirm if it matches 18511446S.
The manufacturer discovered that some of these femoral nails may have been produced with specifications that don't meet quality standards, potentially leading to reduced strength.
Check the product number on the packaging; if it matches 18511446S, contact Stryker for further instructions.
While the recall is for potential reduced strength, the risk of injury is low as the nails are designed for surgical use and breakage is unlikely under normal conditions.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2406-2018 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2406-2018 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.
