Drug recall
v|tome|x L Series non-destructive testing cabinet x-ray systems
FDA recall event 86620 · Class II · Ge Inspection Technologies Llc
Key facts
| Event ID | 86620 |
|---|---|
| Recall numbers | Z-0442-2021 |
| Recalling firm | Ge Inspection Technologies Llc |
| Product type | Devices |
| Products | v|tome|x L Series non-destructive testing cabinet x-ray systems |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | FDA Requested |
| Reason for recall | It was discovered during testing of the v/tome/x L450 system s/n PA1790, that the pre-warning signals does not provide "Audible and visible warning signals within the cabinet" if the "warm up" mode… |
| Initiation date | Sep 29, 2020 |
| Report date | Nov 25, 2020 |
| Termination date | May 2, 2023 |
| City | Skaneateles Falls |
| State | NY |
| Country | United States |
| FEI number | 3004478544 |
At a glance
- 1–9 Products in this recall
- None 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: