FDA Device recall Z-0482-2022
Instavac Portable Suction Pump, Constant mode (model #757000, Instavac C) and Intermittent mode (model 756000, Instavac I)
- FDA Device
- Class II
- ongoing
- Published 2022-01-19
On 2022-01-19 the FDA classified a Class II recall of Instavac Portable Suction Pump, Constant mode (model #757000, Instavac C) and Intermittent mode (model 756000, Instavac I) by Ohio Medical, citing increase in premature device failures.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0482-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2021-11-16 |
| Published | 2022-01-19 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Ohio Medical |
| Distribution | US |
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.
Reason
Increase in premature device failures
Identifiers
| code_info | Shipped between March 2019 and February 2021. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0482-2022%22
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