FDAClass IINovember 13, 2019

Prox Lat Tib Lock Plate and Dist Med Tib Lock Plate recall

Prox Lat Tib Lock Plate and Dist Med Tib Lock Plate Item Nos. 47235700306 47235700308 47235700310 47235700312 47235700314 47235700408 47235700410…

Why was Prox Lat Tib Lock Plate and Dist Med Tib Lock Plate recalled?

Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).

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?

All product manufactured prior to January 2014.

Product
Prox Lat Tib Lock Plate and Dist Med Tib Lock Plate Item Nos. 47235700306 47235700308 47235700310 47235700312 47235700314 47235700408 47235700410…
Recalling firm
Zimmer Biomet, Inc.
Quantity
5,459,583 total devices
Distribution
Distributed nationwide.
Recall date
November 13, 2019
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls