FDAClass IIOctober 22, 2014

Discovery Elbow Humeral Trial Product Usage: Biomet recall

Discovery Elbow Humeral Trial Product Usage: Biomet manufactures a variety of elbow joint replacement prostheses intended for primary and revision…

Why was Discovery Elbow Humeral Trial Product Usage: Biomet recalled?

An investigation identified that the product was incorrectly manufactured as a left humeral trial but is etched as a right humeral trial.

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?

Catalog Number: 414837 Lot Number: 555011

Product
Discovery Elbow Humeral Trial Product Usage: Biomet manufactures a variety of elbow joint replacement prostheses intended for primary and revision…
Recalling firm
Biomet, Inc.
Quantity
6
Distribution
Worldwide Distribution - US Nationwide in the state of SD, OH, CT and the country of: The Netherlands and India.
Recall date
October 22, 2014
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls