Z-1037-2015 Class II Terminated
FDA device recall Z-1037-2015 was initiated by The Anspach Effort, Inc. on Dec 10, 2014 and is designated Class II. Reason for recall: Customer complaint indicating the color bands on the MIA16-G1 were not correct. The recall status is terminated (terminated May 9, 2016). Affected quantity: 8.
Recall Details
- Product Type
- Devices
- Report Date
- Feb 11, 2015
- Initiation Date
- Dec 10, 2014
- Termination Date
- May 9, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 8
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.
Distribution Pattern
US Distribution to the states of: NC and CA., and Internationally to Switzerland.
Code Information
Serial Numbers: H38309606702, H38309606704, H38309610105, H38309610104, H38309606701, H38309606703, H38309606705, H38309610101.
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1037-2015
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026