Device recall
Z-0482-2022: Instavac Portable Suction Pump, Constant mode (model #757000, Instavac C) and…
FDA device recall · Class II · Ohio Medical Corporation
Key facts
| Recall number (Z-number) | Z-0482-2022 |
|---|---|
| Recall event | 88984 |
| Product | Instavac Portable Suction Pump, Constant mode (model #757000, Instavac C) and Intermittent mode (model 756000, Instavac I); and Instavac replacement pumps, part #AI5511, a component of model numbers 756000 and 757000. |
| Product code | BTA |
| Recalling firm | Ohio Medical Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K933902 |
| FEI number | 1419185 |
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