Device recall
Z-0415-05: SSCOR Suction Device Model 2314B
FDA device recall · Class II · S S C O R Inc
Key facts
| Recall number (Z-number) | Z-0415-05 |
|---|---|
| Recall event | 30845 |
| Product | SSCOR Suction Device Model 2314B |
| Product code | BTA |
| Recalling firm | S S C O R Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 13, 2011 |
| FEI number | 2022724 |
At a glance
- None 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