FDA Device recall Z-3211-2017
IMRIS DEERFIELD IMAGING, REF 113803, Starburst adaptor thumb screw
- FDA Device
- Class II
- terminated
- Published 2017-10-04
On 2017-10-04 the FDA classified a Class II recall of IMRIS DEERFIELD IMAGING, REF 113803, Starburst adaptor thumb screw by Deerfield Imaging, citing incorrect thread on thumbscrews.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3211-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-08-14 |
| Published | 2017-10-04 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Deerfield Imaging |
| Distribution | IL, OR, PA |
Product
IMRIS DEERFIELD IMAGING, REF 113803, Starburst adaptor thumb screw
Reason
incorrect thread on thumbscrews
Identifiers
| code_info | Serial Numbers: 10006657, 10006658, 10006725, 10006660, 10006726, 10006659 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3211-2017%22
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