Drug recall
VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001
FDA recall event 98888 · Class II · Ventec Life Systems, Inc.
Key facts
| Event ID | 98888 |
|---|---|
| Recall numbers | Z-2525-2026 |
| Recalling firm | Ventec Life Systems, Inc. |
| Product type | Devices |
| Products | VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which may result in the backup alarm not… |
| Initiation date | May 8, 2026 |
| Report date | Jul 1, 2026 |
| City | Bothell |
| State | WA |
| Country | United States |
| FEI number | 3013095415 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: