Official recall notice
FDA DeviceClass IINotable
FDA Recall: Hintermann Series Talar Implant, Left, Size 2 REF 302112
- Recall date
- 2026-06-17
- Brand
- DT MedTech, LLC
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.
Recommended action
What to do
67 units
Product description
Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.