Recall
FDAHealthMarch 24, 2026

DT MedTech, LLC — Hintermann Series Talar Implant, Left, Size 2 REF 302112

⚠️ Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
March 24, 2026

Worldwide - US Nationwide distribution in the states of CA, AR, AZ, ID and the countries of PER, KOR.

What's affected?

Product
Hintermann Series Talar Implant, Left, Size 2 REF 302112
Lot code
AACAA/

Additional details

Lot: AACAA/ DI: B095302112

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 67 units.

View original FDA notice →

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