Stryker recalls specific femoral nails that were labeled incorrectly as left but contained right nails, or vice versa. This could lead to improper surgical use. Affected items have catalog number 1851-0830S and batch lot K09F17F.
Investigation determined that one lot of the T2 Greater Trochanter Nail (GTN) was labeled as left version but contained a right nail and another lot was labeled as right version but contained a left nail.
Stryker is recalling a specific type of femoral nail that was labeled incorrectly as left but contained a right nail, or vice versa. Using the wrong side could cause improper surgical placement and potential complications during procedures.
The recalled nails were mislabeled: one batch was labeled as left but contained right nails, and another batch was labeled as right but contained left nails. Using the wrong side could lead to improper surgical placement, potentially causing complications during procedures.
Surgical teams using the recalled femoral nails for orthopedic procedures. The risk is highest for surgeons and medical staff handling the specific batch numbers.
Check for the catalog number 1851-0830S and batch lot number K09F17F on the product. The product is a femoral nail, specifically the RIGHT T2 GTN 8x300 mm model.
Look for the catalog number 1851-0830S and batch lot number K09F17F on the nail.
The investigation found that one batch was labeled as left but contained right nails, and another batch was labeled as right but contained left nails.
Check the product label for catalog number 1851-0830S and batch lot K09F17F. If it matches, contact Stryker for guidance.
The recall is for mislabeling that could lead to improper surgical use, but the hazard level is low risk as it does not involve immediate danger 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-1940-2025 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1940-2025 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.
