FDA Device recall Z-1037-2015
16cm Minimally Invasive Attachment
- FDA Device
- Class II
- terminated
- Published 2015-02-11
On 2015-02-11 the FDA classified a Class II recall of 16cm Minimally Invasive Attachment by The Anspach Effort, citing customer complaint indicating the color bands on the MIA16-G1 were not correct.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1037-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-12-10 |
| Published | 2015-02-11 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | The Anspach Effort |
| Distribution | CA, NC |
Product
16cm Minimally Invasive Attachment. For use with Motor Systems for cutting and shaping bones, including the spine and cranium. Model MIA16-G1
Reason
Customer complaint indicating the color bands on the MIA16-G1 were not correct.
Identifiers
| code_info | Serial Numbers: H38309606702, H38309606704, H38309610105, H38309610104, H38309606701, H38309606703, H38309606705, H38309610101. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1037-2015%22
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