Device recall
Z-0921-05: Flexible Implant tube, blind end, 350 mm, part # GM11003730, labeled in part…
FDA device recall · Class II · Varian Medical Systems
Key facts
| Recall number (Z-number) | Z-0921-05 |
|---|---|
| Recall event | 31941 |
| Product | Flexible Implant tube, blind end, 350 mm, part # GM11003730, labeled in part ***Varian Medical Systems, Inc 3100 Hansen Way Palo Alto, CA 94304 USA www.varian.com***. Available as single unit or contained in the Flexible Interstitial Implant Tube Set, part number GM11004680. For use with the Varian… |
| Product code | JAQ |
| Recalling firm | Varian Medical Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 22, 2005 |
| 510(k) numbers | K983436 |
| FEI number | 3000206172 |
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