Stryker recalls LEFT T2 GTN 8x300 mm nails that were mislabeled as left but contained right nails and vice versa. This mix-up could lead to incorrect surgical use.
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 mislabeled. The recall happens because some nails were labeled as left but contained right nails, and vice versa. This mix-up could cause incorrect surgical use during procedures.
The recall involves a mix-up between left and right version nails. This means some products labeled as left contain right nails and vice versa. Using the wrong nail type during surgery could lead to improper implant placement.
Surgical professionals using the recalled femoral nails for orthopedic procedures. Patients receiving these nails during surgery are at risk of incorrect implant placement.
Check for the catalog number 1850-0830S and batch lot number K09F126 on the product. The product is a femoral nail labeled as LEFT T2 GTN 8x300 mm.
Look for the catalog number 1850-0830S and batch lot number K09F126 on the nail packaging.
The recall is because some nails were labeled as left but contained right nails, and vice versa.
Check for the catalog number 1850-0830S and batch lot number K09F126 on the product label.
The recall record does not specify a remedy, so no action is required beyond checking the product label.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1939-2025 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1939-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.