Stryker recalls certain Femoral Nails (A/R T2 Femur 10x340 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, increasing the risk of breaking during use. This could lead to complications in medical procedures if the nail breaks unexpectedly.
The recalled nails may have been produced with specifications that don't meet quality standards. This could cause the nails to become weaker than expected, potentially breaking during surgical procedures.
Medical professionals using the recalled femoral nails for surgeries are most at risk. Patients undergoing procedures with these nails may face complications if the nail breaks unexpectedly.
Check for the product number 18251034S, lot code K0957B1, or GTIN 04546540199508 on the packaging or label. These items were sold with specific dates and locations.
Look for the product number 18251034S, lot code K0957B1, or GTIN 04546540199508 on the packaging or label.
The manufacturer discovered that some products may have been produced outside of specified quality standards, which could lead to reduced strength and premature breakage.
The recall record does not specify a remedy, so check with Stryker directly for guidance.
Check for the product number 18251034S, lot code K0957B1, or GTIN 04546540199508 on the packaging or label.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2395-2018 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2395-2018 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.
