Device recall
Z-1892-2009: BrightView Gamma Camera Radius Drive Assembly, manufactured by Philips Medical…
FDA device recall · Class II · Phillips Nuclear Medicine
Key facts
| Recall number (Z-number) | Z-1892-2009 |
|---|---|
| Recall event | 52704 |
| Product | BrightView Gamma Camera Radius Drive Assembly, manufactured by Philips Medical Systems (Cleveland) Inc., Cleveland, OH, 3/8" tilt, model number 4535604 34811, 3/4"tilt, model number 4535674 34801, and 3/8" fixed, model number 4535604 34781, all catalog number 882480 Medical device-- intended to… |
| Product code | KPS |
| Recalling firm | Phillips Nuclear Medicine |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 12, 2010 |
| 510(k) numbers | K062298 |
| FEI number | 1525965 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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