Device recall
Z-1224-2012: Hamamatsu Corporation, Bridgewater NJ 08807 Microfocus X-ray Source L8601…
FDA device recall · Class II · Hamamatsu Corporation
Key facts
| Recall number (Z-number) | Z-1224-2012 |
|---|---|
| Recall event | 60991 |
| Product | Hamamatsu Corporation, Bridgewater NJ 08807 Microfocus X-ray Source L8601 series, L9121 series (90kV type MICROFOCUS X-RAY SOURCE), L7901 series, and L8031 series (100kV type MICROFOCUS x-ray source |
| Product code | RBS |
| Recalling firm | Hamamatsu Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 29, 2018 |
| FEI number | 1000121818 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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