DT MedTech Hintermann Talar Implant Left-Size 4: Incorrect Labeling Recall

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Recalling firmDT MedTech, LLC110 West Rd Ste 227 · Towson, MD 21204-2341

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✎ GovInfoNow plain-language explainer

What happened, in plain English

DT MedTech is recalling LEFT-SIZE 4 Talar Implant components (part number 302114) because the packaging labels incorrectly identify the device size. This could lead to improper use if the wrong size is selected during surgery.

Why it’s dangerous

Incorrect labeling means the device might be misidentified as a different size during surgery. This could lead to improper implantation if the wrong size is used, potentially causing complications.

Who’s affected

Surgical teams and patients using DT MedTech's LEFT-SIZE 4 Talar Implant components (part 302114) for mobile ankle joint prostheses. Surgeons and medical facilities are most at risk.

How to tell if you have this one

Check for part number 302114 on the packaging. The product is labeled as 'LEFT-SIZE 4 Talar Implant' for mobile ankle joint prostheses. Lot number AAAEM is associated with this recall.

Brand
DT MedTech
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Labeling
Verify the part number on the packaging is 302114 and the product is labeled as 'LEFT-SIZE 4 Talar Implant' for mobile ankle joint prostheses.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

The packaging labels incorrectly identify the device size, which could lead to improper use during surgery.

What is the part number for this recall?

Part number 302114 for the LEFT-SIZE 4 Talar Implant components.

Is there a fix for this issue?

The official recall does not provide a remedy, so no action is required beyond checking the labeling.

Take action

Contact DT MedTech

We’ve drafted a message you can send DT MedTech to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0403-2019 — DT MedTech DT MedTech

Hello,

I own a DT MedTech that is covered by recall Z-0403-2019 from DT MedTech.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-0403-2019 (September 25, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0403-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

DT MedTech, LLC recalls DT Medi Tech Hintermann Series Talar Implant LEFT-SIZE 4 Part Number: 302114 components are prostheses for a mobile

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