Stryker recalls certain Femoral Nails (A/R T2 Femur 10x320 mm) due to potential reduced strength causing premature breakage. Affected units 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, increasing the risk of breaking during use. This could lead to complications in medical procedures if the nail fractures unexpectedly.
The nails may have been produced with specifications that don't meet quality standards. This could cause the nails to become weaker than intended, potentially breaking during surgical procedures.
Medical professionals using the recalled femoral nails for surgeries are most at risk. Patients receiving these nails during procedures may also be affected if the nail breaks unexpectedly.
Check for the product number 18251032S, lot code K081642, or GTIN 04546540199492 on the nail packaging. These items were sold with specific dates and locations.
Verify the product number, lot code, and GTIN on the nail packaging to confirm if it's affected.
Stryker discovered that some of these femoral nails may have been produced with specifications that don't meet quality standards, potentially causing reduced strength and premature breakage.
Look for the product number 18251032S, lot code K081642, or GTIN 04546540199492 on the nail packaging.
The recall record does not specify a remedy, so contact Stryker directly for guidance on next steps.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2394-2018 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2394-2018 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.
