FDAMarch 24, 2026device

Hintermann Series Talar Implant, Left, Size 2 REF 302112

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Ongoing

Brands named

dt medtech

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →