Device recall
Z-3211-2017: IMRIS DEERFIELD IMAGING, REF 113803, Starburst adaptor thumb screw
FDA device recall · Class II · Deerfield Imaging
Key facts
| Recall number (Z-number) | Z-3211-2017 |
|---|---|
| Recall event | 77996 |
| Product | IMRIS DEERFIELD IMAGING, REF 113803, Starburst adaptor thumb screw |
| Product code | HBL |
| Recalling firm | Deerfield Imaging |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 29, 2018 |
| 510(k) numbers | K103493 |
| FEI number | 3010326005 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database