Device recall
Z-1020-2009: Spacers of varying lengths used with the InSTANT Stranding System, Part numbers…
FDA device recall · Class II · Theragenics Corporation
Key facts
| Recall number (Z-number) | Z-1020-2009 |
|---|---|
| Recall event | 51177 |
| Product | Spacers of varying lengths used with the InSTANT Stranding System, Part numbers: TG3138, TG3139, TG3140, TG3141 and TG3142. Theragenics Corporation, 5203 Bristol Industrial Way, Buford GA 30518. The spacer product is intended for consumption during the brachytherapy procedure. Unused (unopened)… |
| Product code | NQO |
| Recalling firm | Theragenics Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 6, 2009 |
| 510(k) numbers | K072296 |
| FEI number | 1037598 |
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