Drug recall
Discovery NM 630 Model # H3101RH
FDA recall event 86337 · Class II · GE Healthcare, LLC
Key facts
| Event ID | 86337 |
|---|---|
| Recall numbers | Z-2991-2020, Z-2992-2020, Z-2993-2020, Z-2994-2020, Z-2995-2020, Z-2997-2020, Z-2998-2020 |
| Recalling firm | GE Healthcare, LLC |
| Product type | Devices |
| Products | Discovery NM 630 Model # H3101RH, Discovery NM670 Pro Model # H3100XB, NM 830 Model # H3910AC, NM/CT 850 Model Number: H3907AD, NM/CT 860, SPECT/CT and 2 more |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Rotor bearing screws were found loose on detector. |
| Initiation date | Aug 14, 2020 |
| Report date | Sep 30, 2020 |
| Termination date | May 6, 2021 |
| City | Waukesha |
| State | WI |
| Country | United States |
| FEI number | 2126677 |
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: