DT MedTech, LLC recalls Hintermann Series Talar Implant
- Recalling company
- DT MedTech, LLC
- Product
- Hintermann Series Talar Implant, Left, Size 2 REF 302112
- Reason
- Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Mar 24, 2026
- Reported
- Jun 17, 2026
- Distribution
- Worldwide - US Nationwide distribution in the states of CA, AR, AZ, ID and the countries of PER, KOR.
- Status
- Ongoing
- Quantity
- 67 units
- Lot / codes
- Lot: AACAA/ DI: B095302112
- Company location
- Mcminnville, TN
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2399-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2399-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.