Hintermann Series Talar Implant — Class II medical device recall Z-2399-2026
Ongoing recall by DT MedTech, LLC, reported 2026-06-17, distributed nationwide. Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant
| Recall number | Z-2399-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | DT MedTech, LLC, Mcminnville, TN, United States |
| Recall initiated | 2026-03-24 |
| Classified | 2026-06-10 |
| Reported by FDA | 2026-06-17 |
| Distributed | Nationwide (US) |
| Quantity | 67 units |
| Reason classes | labeling |
| Model numbers | 302112 |
Product
Hintermann Series Talar Implant, Left, Size 2 REF 302112
Reason for recall
Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2399-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.