FDAClass IIMay 23, 2018

Epic Extremity Plate System recall

Epic Extremity Plate System, Midfoot/Flatfoot Insert, Part 2111-0005 with Extended Butterfly Plate (2000-5002)

Why was Epic Extremity Plate System recalled?

There is an error in the caddy artwork that misidentifies a specific plate and screw.

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: 2111-0005 Lot: 51464

Product
Epic Extremity Plate System, Midfoot/Flatfoot Insert, Part 2111-0005 with Extended Butterfly Plate (2000-5002)
Recalling firm
Epic Extremity, LLC
Quantity
6 units
Distribution
The products were distributed to the following US states: FL, PA, and VA.
Recall date
May 23, 2018
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls