Device recall
Z-0974-05: PG910 Spacers, Part number SP101, loaded into Bard Express Seeding Cartridges…
FDA device recall · Class III · Theragenics Corporation
Key facts
| Recall number (Z-number) | Z-0974-05 |
|---|---|
| Recall event | 32194 |
| Product | PG910 Spacers, Part number SP101, loaded into Bard Express Seeding Cartridges containing TheraSeed Pd-103 devices. The product is shipped non-sterile in a foil pouch, packed 50 loose spacers per pouch. |
| Product code | KXK |
| Recalling firm | Theragenics Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 5, 2005 |
| FEI number | 1037598 |
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