Stryker GmbH has recalled 3 units of the T2 Greater Trochanter Nail (GTN), a femoral surgical implant. The recall was initiated because one lot of these surgical nails was labeled as the "left" version but contained a "right" nail, while another lot was labeled as the "right" version but contained a "left" nail. No injuries or incidents have been reported to date.
If a surgeon attempts to use the incorrectly labeled nail during a procedure, it could lead to surgical delays while the correct part is located or potential complications if the mismatched implant is not identified. Surgical staff should verify product orientation before use.
Recall Number: Z-1939-2025
Recall Number: Z-1940-2025
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
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