Drug recall
Hintermann Series Talar Implant, Left, Size 2 REF 302112
FDA recall event 98987 · Class II · DT MedTech, LLC
Key facts
| Event ID | 98987 |
|---|---|
| Recall numbers | Z-2399-2026 |
| Recalling firm | DT MedTech, LLC |
| Product type | Devices |
| Products | Hintermann Series Talar Implant, Left, Size 2 REF 302112 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Mar 24, 2026 |
| Report date | Jun 17, 2026 |
| City | Mcminnville |
| State | TN |
| Country | United States |
| FEI number | 3012104767 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: