16cm Minimally Invasive Attachment — Class II medical device recall Z-1037-2015
Terminated recall by The Anspach Effort, Inc., reported 2015-02-11, distributed in CA, NC. Customer complaint indicating the color bands on the MIA16-G1 were not correct.
| Recall number | Z-1037-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | The Anspach Effort, Inc., Palm Beach Gardens, FL, United States |
| Recall initiated | 2014-12-10 |
| Classified | 2015-02-04 |
| Reported by FDA | 2015-02-11 |
| Terminated | 2016-05-09 |
| Distributed | CA, NC |
| Countries outside the US | CH |
| Quantity | 8 |
| Serial numbers | H38309606701, H38309606702, H38309606703, H38309606704, H38309606705, H38309610101, H38309610104, H38309610105 |
| Model numbers | MIA16-G1 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1037-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.