FDAClass IINovember 14, 2018

DT Medi Tech Hintermann Series Talar Implant LEFT-SIZE recall: Labeling Error

DT Medi Tech Hintermann Series Talar Implant LEFT-SIZE 4 Part Number: 302114 components are prostheses for a mobile bearing ankle joint.

Why was DT Medi Tech Hintermann Series Talar Implant LEFT-SIZE recalled?

Incorrect package labeling identifying the device

What should I do if I have this product?

Review the official FDA enforcement record for current 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: AAAEM

Product
DT Medi Tech Hintermann Series Talar Implant LEFT-SIZE 4 Part Number: 302114 components are prostheses for a mobile bearing ankle joint.
Recalling firm
DT MedTech, LLC
Quantity
1
Distribution
Australia, Ireland, Korea, Germany
Recall date
November 14, 2018
Classification
Class II
Status
Terminated
Agency
FDA (device)
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