Drug recall
Invivo Corporation Expression MRI Patient Monitoring System. The Expression MRI Patient Monitoring System is…
FDA recall event 63643 · Class II · Invivo Corporation
Key facts
| Event ID | 63643 |
|---|---|
| Recall numbers | Z-0468-2013 |
| Recalling firm | Invivo Corporation |
| Product type | Devices |
| Products | Invivo Corporation Expression MRI Patient Monitoring System. The Expression MRI Patient Monitoring System is intended for use by healthcare professionals to monitor vital signs for patients undergoing… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Invivo Corporation located at 12151 Research Parkway, Orlando, FL 32826 is recalling the Expression MRI Patient Monitoring System because during transport of the system s cart with a docked Display… |
| Initiation date | Oct 15, 2012 |
| Report date | Dec 12, 2012 |
| Termination date | Feb 13, 2015 |
| City | Orlando |
| State | FL |
| Country | United States |
| FEI number | 1051786 |
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: