Drug recall
GM60A. Digital Diagnostic Mobile X-Ray System.
FDA recall event 95100 · Class II · NeuroLogica Corporation
Key facts
| Event ID | 95100 |
|---|---|
| Recall numbers | Z-2715-2024 |
| Recalling firm | NeuroLogica Corporation |
| Product type | Devices |
| Products | GM60A. Digital Diagnostic Mobile X-Ray System. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Potential for the anti-fall system of the device arm to fail. |
| Initiation date | Jul 8, 2024 |
| Report date | Aug 28, 2024 |
| City | Danvers |
| State | MA |
| Country | United States |
| FEI number | 3004938766 |
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: