Towson, MD, United States
DT MedTech, LLC recalls
2 recalls recorded since 2018, most recently on 24 March 2026. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls2
Ongoing (FDA)1
Terminated or completed1
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 24 March 2026
- Reason
- Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.
- Distribution
- Worldwide - US Nationwide distribution in the states of CA, AR, AZ, ID and the countries of PER, KOR.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2399-2026
- Hintermann Series Talar Implant, Left, Size 2 REF 302112
Terminated Class II Medical devices
- Recall started
- 25 September 2018
- Terminated
- 5 December 2019
- Reason
- Incorrect package labeling identifying the device
- Distribution
- Australia, Ireland, Korea, Germany
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-0403-2019, Z-0402-2019
- DT Medi Tech Hintermann Series Talar Implant LEFT-SIZE 4 Part Number: 302114 components are prostheses for a mobile bearing ankle joint.
- DT Medical -Hintermann Series H3 Poly Inlay, Size 3 5mm Part Number: 300305 components are prostheses for a mobile bearing ankle joint.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.