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Open, Classified

Hintermann Series Talar Implant, Left, Size 2 REF 302112

FDA Recall Z-2399-2026 · Posted 2026-06-10

Recalling FirmDT MedTech, LLC
Recall StatusOpen, Classified
Product CodeNTG
Date Initiated2026-03-24
Product Quantity67 units

Reason for Recall

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

Firm Action

On March 24, 2026, DT MedTech issued a Urgent Medical Device Recall Notification to affected consignees. DT MedTech requested that the firm take the following actions: 1. Return of all available stock of Hintermann Series Talar Implants (Part/REF number 302112, Lot number AACAA) 2. Please provide confirmation that all available stock of the part detailed below has been returned to Vilex LLC at 4516 S 700 E Suite 100A Salt Lake City, Utah 84107 USA. 3. For any questions or concerns, contact Vilex Quality at [email protected] or 800-521-5002.

Root Cause

Labeling Change Control

Distribution Pattern

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

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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