medical MODERATE Updated 2026-06-17

DT MedTech, LLC recalls Hintermann Series Talar Implant, Left, Size 2 REF 302112

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Recalled Product

Hintermann Series Talar Implant, Left, Size 2 REF 302112

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Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot: AACAA/ DI: B095302112

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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