Drug recall
Medrad Continuum MR Infusion system- non-wireless system The MEDRAD Continuum MR Infusion System is designed…
FDA recall event 68293 · Class II · Bayer Corp
Key facts
| Event ID | 68293 |
|---|---|
| Recall numbers | Z-1673-2014 |
| Recalling firm | Bayer Corp |
| Product type | Devices |
| Products | Medrad Continuum MR Infusion system- non-wireless system The MEDRAD Continuum MR Infusion System is designed for patients who require medications and other fluids during an MR procedure. It is… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | There is a potential safety risk associated with potentially damaged locking pins within the bracket of non-wireless versions of Continuum systems shipped prior to March 2008. |
| Initiation date | Apr 3, 2014 |
| Report date | Jun 11, 2014 |
| Termination date | Apr 16, 2015 |
| City | Warrendale |
| State | PA |
| Country | United States |
| FEI number | 3009621430 |
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: