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DT MedTech, LLC recalls DT Medical -Hintermann Series H3 Poly Inlay, Size 3 5mm Part Number: 300305 components are prostheses for a mobile bea
Recalled November 14, 2018 · FDA recall Z-0402-2019 · DT MedTech
Hazard
Incorrect package labeling identifying the device · FDA Class II
Units
54 units
Sold at
Australia, Ireland, Korea, Germany
Description
Incorrect package labeling identifying the device
Product
DT Medical -Hintermann Series H3 Poly Inlay, Size 3 5mm Part Number: 300305 components are prostheses for a mobile bearing ankle joint.
Manufacturer(s)
DT MedTech, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →