Drug recall
Monaco RTP System Radiation treatment planning
FDA recall event 65996 · Class II · Elekta, Inc.
Key facts
| Event ID | 65996 |
|---|---|
| Recall numbers | Z-2276-2013 |
| Recalling firm | Elekta, Inc. |
| Product type | Devices |
| Products | Monaco RTP System Radiation treatment planning |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Upgrade installation script is designed to overwrite the same pouch files in the Treatment Couch Library with the original default values. |
| Initiation date | Jul 2, 2013 |
| Report date | Oct 2, 2013 |
| Termination date | May 8, 2014 |
| City | Atlanta |
| State | GA |
| Country | United States |
| FEI number | 1037831 |
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: