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Waldemar Link GmbH & Co. KG (Mfg Site) recalls LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Left
Recalled July 5, 2023 · FDA recall Z-2049-2023 · Waldemar Link GmbH & Co. KG (Mfg Site)
Hazard
The firm discovered through customer complaints that device segments may not meet specifications. · FDA Class II
Units
13 units
Sold at
Domestic: AL, GA, IL, IN, KS, NJ, NY, and TX. Foreign: Argentina, Australia, Austria, Brazil, Finland, France, Germany, India, Italy, Spain, and United Kingdom.
Description
The firm discovered through customer complaints that device segments may not meet specifications.
Product
LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Left
Manufacturer(s)
Waldemar Link GmbH & Co. KG (Mfg Site)
Made in
Germany
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →