DT MedTech recalls

Recall found. DT MedTech is named in FDA Class II recall Z-2399-2026 covering Hintermann Series Talar Implant. Hazard: Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device. Identifying details: Lot: AACAA/ DI: B095302112. Status: Ongoing.

Models with recalls

Hintermann Series Talar Implant (1)

All DT MedTech recalls

FDA Class II · Medical device · June 17, 2026

Hintermann Series Talar Implant recall — DT MedTech, LLC

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

Official ID Z-2399-2026 · Official record ↗

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CPSC — consumer products ↗ (aggregated here)
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FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.