FDA Recall Terminated

MaxAn 4.0mm and 4.5mm fixed screws, used in the MaxAn Anterior Cervical Plate System. The MaxAn Anterior Cervical Plate System is a decompression-based technique for cervical spine stabilization.

Recall: Z-0203-2016 · Initiated September 29, 2015

Recall

Recall Number
Z-0203-2016
Event Number
72312
Firm
Biomet Spine, LLC
FEI Number
3012447612
Product Code
KWQ
Status
Terminated
Root Cause
Labeling mix-ups
Initiated
September 29, 2015
Posted
November 3, 2015
Terminated
April 29, 2016
Address
310 Interlocken Pkwy, Ste 120, Broomfield, CO, 80021-3464

Description

MaxAn 4.0mm and 4.5mm fixed screws, used in the MaxAn Anterior Cervical Plate System. The MaxAn Anterior Cervical Plate System is a decompression-based technique for cervical spine stabilization.

Reason

The packaging of 4.5 mm diameter MaxAn screws identifies/labels the screws as 4.0 mm diameter screws.

Action

Zimmer Biomet Spine sent an Urgent Medical Device Recall Notice dated September 29, 2015, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer. If the device has already been implanted, written confirmation of this will be required and the necessary parties will be contacted. They will store returned product in quarantine in an isolated location until they can undergo inspection to verify if they are conforming or not and then will be destroyed or retained. Necessary parts will be destroyed so that it is visually obvious they are no longer functional. For further questions call (303) 443-7500 ext.244.

Distribution

US Distribution to the states of : NY, MO, and FL

Quantity

17 units