FDA Medical devices recall ·
Hintermann Series Talar Implant, Left, Size 2 recall
- Recall number
- Z-2399-2026
- Date
- (initiated March 24, 2026)
- Company / brand
- DT MedTech, LLC
111 Moffitt St, Mcminnville, TN, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 67 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Hintermann Series Talar Implant, Left, Size 2 REF 302112
Why was it recalled?
Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot: AACAA/ DI: B095302112
Distribution
Worldwide - US Nationwide distribution in the states of CA, AR, AZ, ID and the countries of PER, KOR.
States: Arkansas Arizona California Idaho
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2399-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.