Class II

Medical Device Recall: Hintermann Series Talar Implant, Left, Size 2 REF 302112

DT MedTech, LLC · March 24, 2026

Reason for Recall

Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.

Distribution

Worldwide - US Nationwide distribution in the states of CA, AR, AZ, ID and the countries of PER, KOR.

States Affected

NATIONWIDE

Quantity Affected

67 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2399-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.