FDAFDA · Food and drugs·Recall number Z-2399-2026
Hintermann Series Talar Implant, Left, Size 2 REF 302112
Published June 17, 2026 · Recall initiated: March 24, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- DT MedTech, LLC
- Distributor
- Worldwide - US Nationwide distribution in the states of CA, AR, AZ, ID and the countries of PER, KOR.
- Lot
- Lot: AACAA/ DI: B095302112
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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