Hintermann Series Talar Implant recall (DT MedTech, LLC)
Medical deviceClass IIOngoing
Summary: DT MedTech, LLC is recalling 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.
What is being recalled
Hintermann Series Talar Implant, Left, Size 2 REF 302112
Why
Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
Worldwide - US Nationwide distribution in the states of CA, AR, AZ, ID and the countries of PER, KOR. (states named: Arkansas, Arizona, California, Idaho)
How to tell if yours is affected
Lot: AACAA/ DI: B095302112
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-2399-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | March 24, 2026 |
| Reported | June 17, 2026 |
| Company | DT MedTech, LLC |
| Company location | Mcminnville, TN, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 67 units |
More recalls from DT MedTech, LLC · all medical device recalls · recalls from March 2026