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Recall Observatory FDA recall evidence

Device product

CardioQuip, Modular Cooler-Heater 1000(i), Refrigeration Module, Model: MCH-10RMS, UDI: (01)00860000846127 used with heat exchange devices.

Z-0069-2022

June 24, 2021

Class II

Product summary

Firm
CardioQuip, LLC
Event
Event 88621
Status
Ongoing
Classification
Class II
Quantity
1380 units
Official record key
device-enforcement:Z-0069-2022

Official wording

Reason: There is the potential bacterial including Nontuberculous mycobacterial (NTM) to grow in the water system of heater-cooler devices which could result in contaminated water potentially aerosolized into the operating room during surgery which could result in patient infection.

Code information: All Serial Numbers

Distribution pattern: Worldwide distribution - US Nationwide distribution including in the states of TX, PA, FL, CA, HI, SC, OH, AK, NY, IL, AR, WI, MI, AL, KS, NJ, GA, AZ, KY, MS, TN, LA, DE, MA, VA, CO, NE, NC, NH, ME, WV, PA, MO, MN, IN, CT, NH, NV, UT and the country of Venezuela.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    There is the potential bacterial including Nontuberculous mycobacterial (NTM) to grow in the water system of heater-cooler devices which could result in contaminated water potentially aerosolized into the operating room during surgery which could result in patient infection.