Stryker Corporation is recalling 860 units of its Precision Thin Micro Oscillating and Sagittal Blades because the attachments may be out of measurement specifications. This manufacturing defect prevents the blades from fitting securely into the compatible surgical handpiece. No injuries have been reported to date. If you work in a clinical or hospital setting, please contact the manufacturer or your distributor to arrange for a return or replacement.
The blades may fail to fit securely or could detach from the surgical handpiece during a procedure. This poses a risk of surgical delays or injury to the patient or surgical staff if the blade becomes loose during use.
Clinical Device Correction/Return
Recall #: Z-1138-2025
Recall #: Z-1139-2025
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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