Hintermann Series Talar Implant recall: Labeling Error
Hintermann Series Talar Implant, Left, Size 2 REF 302112
Why was Hintermann Series Talar Implant 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 I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot: AACAA/ DI: B095302112
- Product
- Hintermann Series Talar Implant, Left, Size 2 REF 302112
- Recalling firm
- DT MedTech, LLC
- Quantity
- 67 units
- Distribution
- Worldwide - US Nationwide distribution in the states of CA, AR, AZ, ID and the countries of PER, KOR.
- Recall date
- June 17, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)