Waldemar Link GmbH & Co. KG (Mfg Site) has recalled 109 units of its Modular Stem cylindrical Tilastan press-fit cementless implants. The recall includes 80 mm length stems in 11 mm, 12 mm, and 13 mm diameters. These products were recalled because the Global Trade Item Number (GTIN) on the outer carton label is incorrect and belongs to a different product. No injuries or incidents have been reported in connection with this labeling error.
The incorrect barcode and labeling on the outer packaging could lead a surgical team to select or prepare the wrong size or type of implant for a patient. This mismatch may result in surgical delays or medical complications if the incorrect part is used or needs to be swapped during a procedure.
Manufacturer initiated recall via notification letter.
Recall #: Z-1372-2025; Quantity: 37 units
Recall #: Z-1373-2025; Quantity: 52 units
Recall #: Z-1374-2025; Quantity: 20 units
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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