FDAClass IIMay 24, 2017

Biomet Microfixation TraumaOne System Surgical Tray recall

Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600

Why was Biomet Microfixation TraumaOne System Surgical Tray recalled?

Part of the number on the tray lid differ from the part number on the base.

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?

Part Number 46-1610 // Lot Number 709730 Part Number 46-1610 // Lot Number 709740 Part Number 46-1620 // Lot Number 709710 Part Number 46-1620 // Lot Number 709720

Product
Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600
Recalling firm
Biomet Microfixation, LLC
Quantity
33 units
Distribution
AL, MO and UT Canada, Australia, Netherlands, and Egypt
Recall date
May 24, 2017
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls