Device recall
Z-2765-2016: SureSight Obturator Introducer Localization Systems (ILS) for ATEC in MRI…
FDA device recall · Class II · Hologic, Inc
Key facts
| Recall number (Z-number) | Z-2765-2016 |
|---|---|
| Recall event | 74839 |
| Product | SureSight Obturator Introducer Localization Systems (ILS) for ATEC in MRI. ILS-0914-20-OB (9G Introducer Localization Set (OB Model) for ATEC0914-20MR Handpiece) |
| Product code | GDF |
| Recalling firm | Hologic, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 30, 2017 |
| FEI number | 1000120743 |
At a glance
- None 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