Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include guidance for proper water-quality...
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 CardioQuip, LLC directly.
Affected Products
CardioQuip, Modular Cooler-Heater 1000(m),Compact Unit, Model:MCH-1000(m),CE 2797, UDI: (01)00860000846110
Quantity: 1646 units
Why Was This Recalled?
Labeling does not include guidance for proper water-quality maintenance and device inspection for heater cooler devices.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About CardioQuip, LLC
CardioQuip, LLC has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report