Medrad Inc Recall: Medrad(R) Continuum MR Infusion System Secondary Administration Kit Pe
Medrad Inc Recall: Medrad(R) Continuum MR Infusion System Secondary Administration Kit Pe is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Medrad Inc; Product: Medrad(R) Continuum MR Infusion System Secondary Administration Kit Peristaltic Pump System designed for patients who require m
| Recalling firm | Medrad Inc |
|---|---|
| Product | Medrad(R) Continuum MR Infusion System Secondary Administration Kit Peristaltic Pump System designed for patients who require medications and other fluids during an MR procedure. It is intended to provide infusion therapy directly prior to, during and immediately after the MR procedure functioning while either stationary or mobile. |
| Reason for recall | Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System tubing sets (macrobore and microbore), catalog numbers MIK200A, MIL 200B, 3015153, 3015155, 3015156, 3015157, 3015158, 3015159, and 3015161. The firm is initiating this recall because this tubing exhibits a variation that, when used in conjunction with any Continuum pump, may result in flow rate accuracy performance issues. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Worldwide distribution: USA (nationwide) and countries of: Australia, Bermuda, Brazil, Canada, China, Chile, Denmark, Dominican Republic, Estonia, Finland, France, Germany, Great Britain, Guam, Hong Kong, India, Israel, Italy, Japan, Korea, Lebanon, Mexico, Malaysia, Netherland, Poland, Portugal, Pu |
| Recall initiated | 20120418 |
| Recall number | Z-0597-2013 |
| Category | device |
| State | PA |
| Country | United States |
$29/mo
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