Drug recall
GlideScope Go Monitors
FDA recall event 88214 · Class III · Verathon, Inc.
Key facts
| Event ID | 88214 |
|---|---|
| Recall numbers | Z-2172-2021 |
| Recalling firm | Verathon, Inc. |
| Product type | Devices |
| Products | GlideScope Go Monitors |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Handheld video monitor failed to meet the labeled IP67 rating which may allow fluid ingress into the monitor resulting in loss of functionality. |
| Initiation date | Jul 1, 2021 |
| Report date | Aug 11, 2021 |
| City | Bothell |
| State | WA |
| Country | United States |
| FEI number | 3022472 |
At a glance
- 1–9 Products in this recall
- 10–99 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: