IMRIS DEERFIELD IMAGING — Class II medical device recall Z-3211-2017
Terminated recall by Deerfield Imaging, reported 2017-10-04, distributed in IL, OR, PA. incorrect thread on thumbscrews
| Recall number | Z-3211-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Deerfield Imaging, Minnetonka, MN, United States |
| Recall initiated | 2017-08-14 |
| Classified | 2017-09-22 |
| Reported by FDA | 2017-10-04 |
| Terminated | 2018-05-29 |
| Distributed | IL, OR, PA |
| Quantity | 6 screws |
| Serial numbers | 10006657, 10006658, 10006659, 10006660, 10006725, 10006726 |
| Model numbers | 113803 |
Product
IMRIS DEERFIELD IMAGING, REF 113803, Starburst adaptor thumb screw
Reason for recall
incorrect thread on thumbscrews
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-3211-2017. 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.