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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.

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
March 24, 2026
Status
ACTIVE

Quick Facts at a Glance

Recall Date
March 24, 2026
Hazard Level
HIGH
Brand
DT MedTech
Geographic Scope
1 states

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
DT MedTech
Model numbers
Lot: AACAA/ DI: B095302112
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    March 24, 2026

  2. Reported by FDA DEVICE

    June 17, 2026

  3. RecallRadar source check

    June 23, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

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

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact DT MedTech, LLC or your healthcare provider for instructions. Notification method: E-Mail

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Full Description

Hintermann Series Talar Implant, Left, Size 2 REF 302112. Reason: Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.. Classification: Class II. Quantity: 67 units. Distribution: Worldwide - US Nationwide distribution in the states of CA, AR, AZ, ID and the countries of PER, KOR.

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
Lot: AACAA/ DI: B095302112
Affected States
ALL
Report Date
June 17, 2026
Recall Status
ACTIVE