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Recall Observatory FDA recall evidence

Device product

CardioQuip, Modular Cooler-Heater 1000(m),Compact Unit, Model:MCH-1000(m),CE 2797, UDI: (01)00860000846110

Z-0037-2022

May 12, 2021

Class II

Product summary

Firm
CardioQuip, LLC
Event
Event 88622
Status
Ongoing
Classification
Class II
Quantity
1646 units
Official record key
device-enforcement:Z-0037-2022

Official wording

Reason: Labeling does not include guidance for proper water-quality maintenance and device inspection for heater cooler devices.

Code information: All Serial numbers

Distribution pattern: Worldwide distribution - US Nationwide distribution in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV and the countries of Germany, The Bahamas, Panama, Uruguay.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Labeling does not include guidance for proper water-quality maintenance and device inspection for heater cooler devices.