FDAClass IIJuly 11, 2018

Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ recall

Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 10; 00-7713-010-00

Why was it recalled?

The source record does not provide a concise hazard summary.

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?

62361460 62528141

Product
Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 10; 00-7713-010-00
Recalling firm
Zimmer Biomet, Inc.
Quantity
24
Distribution
Products were distributed solely to Japan.
Recall date
July 11, 2018
Classification
Class II
Status
Terminated
Agency
FDA (device)
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