Waldemar Link GmbH & Co. KG (Mfg Site) recalls LINK Endo-Model Modular Knee Prosthesis System Femoral Segme
Recalled Product
LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Left
Hazard / Issue
The firm discovered through customer complaints that device segments may not meet specifications.
Issued by
FDA
Affected States: AL, GA, IL, IN, KS, NJ, NY, TX
Lot/Code Info: Item No. 15/2973/06; UDI-DI: 04026575340736.
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