Stryker recalls specific femoral nails due to potential reduced strength causing premature breakage. Affected products have Product Number 18510932S and Lot code K076A80.
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 break prematurely due to manufacturing issues. This could lead to complications during medical procedures if the nail fails unexpectedly.
The recalled femoral nails may have weaker strength due to manufacturing defects. This could cause the nails to break prematurely during surgical procedures, potentially leading to complications for patients.
Medical professionals using the recalled femoral nails for surgeries are affected. Patients undergoing procedures with these nails face potential complications if the nail breaks unexpectedly.
Check for Product Number 18510932S and Lot code K076A80 on the nail packaging. The product is a femoral nail with a size of 9x320 mm.
Verify the product number and lot code on the nail packaging to confirm if it's affected.
The manufacturer discovered that some products may have been made outside specifications, which could lead to reduced strength and premature breakage.
Check the product number and lot code on the packaging. If it matches the recalled items, stop using it and contact Stryker for further instructions.
The recall is for potential premature breakage during surgery, which could lead to complications but does not indicate a risk of serious injury in normal use.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2405-2018 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2405-2018 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.
