Z-0597-2013 Class II Terminated
Recall Details
- Product Type
- Devices
- Report Date
- December 26, 2012
- Initiation Date
- April 18, 2012
- Termination Date
- August 17, 2015
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1,229 Pumps total
Product Description
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.
Distribution Pattern
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, Puerto Rico, Sweden, Singapore, Taiwan, Thailand, and Venezula.
Code Information
Catalog number - Secondary Kit: MIL 200B. See firm's website - www.medrad.com for specific serial and lot numbers.