Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Medrad Continuum MR Infusion system- non-wireless system The MEDRAD Continuum Recalled by Bayer Corp Due to There is a potential safety risk associated with...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Bayer Corp directly.
Affected 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 intended to provide infusion therapy directly prior to, during and immediately after the MR procedure functioning while either stationary or mobile. It is not intended to provide long-term patient care outside the MR environment. The system is to be used by trained medical staff, primarily critical care, emergency room and radiology nursing staff.
Quantity: 1347
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bayer Corp
Bayer Corp has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report