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DT MedTech, LLC recalls Hintermann Series Talar Implant, Left, Size 2 REF 302112
Recalled June 17, 2026 · FDA recall Z-2399-2026 · DT MedTech
Hazard
Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device. · FDA Class II
Units
67 units
Sold at
Worldwide - US Nationwide distribution in the states of CA, AR, AZ, ID and the countries of PER, KOR.
Description
Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.
Product
Hintermann Series Talar Implant, Left, Size 2 REF 302112
Manufacturer(s)
DT MedTech, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →