Device recall
Z-0745-04: RAD SOURCE RS 3000 Blood Irradiator Three Bag Option
FDA device recall · Class III · Rad-Source Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-0745-04 |
|---|---|
| Recall event | 26998 |
| Product | RAD SOURCE RS 3000 Blood Irradiator Three Bag Option |
| Product code | MOT |
| Recalling firm | Rad-Source Technologies, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 3, 2012 |
| 510(k) numbers | K974210 |
| FEI number | 3002459090 |
At a glance
- 1–9 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