Z-0600-2013 Class II Terminated

Recalled by Medrad Inc — Indianola, PA

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 Primary VSA Set 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 - Primary VSA Set: 3015157. See firm's website - www.medrad.com for specific serial and lot numbers.