Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Medrad(R) Continuum MR Infusion System Standard Administration Kit Peristaltic Pump Recalled by Medrad Inc Due to Bayer HealthCare is recalling all MEDRAD(R) Continuum MF...
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 Medrad Inc directly.
Affected Products
Medrad(R) Continuum MR Infusion System Standard 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.
Quantity: 1,229 Pumps total
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medrad Inc
Medrad Inc has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report