PlainRecalls
FDA Devices Moderate Class II Terminated

16cm Minimally Invasive Attachment. For use with Motor Systems for cutting and shaping bones, including the spine and cranium. Model MIA16-G1

Reported: February 11, 2015 Initiated: December 10, 2014 #Z-1037-2015

Product Description

16cm Minimally Invasive Attachment. For use with Motor Systems for cutting and shaping bones, including the spine and cranium. Model MIA16-G1

Reason for Recall

Customer complaint indicating the color bands on the MIA16-G1 were not correct.

Details

Recalling Firm
The Anspach Effort, Inc.
Units Affected
8
Distribution
US Distribution to the states of: NC and CA., and Internationally to Switzerland.
Location
Palm Beach Gardens, FL

Frequently Asked Questions

What product was recalled?
16cm Minimally Invasive Attachment. For use with Motor Systems for cutting and shaping bones, including the spine and cranium. Model MIA16-G1. Recalled by The Anspach Effort, Inc.. Units affected: 8.
Why was this product recalled?
Customer complaint indicating the color bands on the MIA16-G1 were not correct.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 11, 2015. Severity: Moderate. Recall number: Z-1037-2015.