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

Recall number

Z-0069-2022

Recalling firm

CardioQuip, LLC

Product

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

Status

Open, Classified

Initiated

2021-06-24

Posted

not on file

Terminated

not on file

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.

Root cause

Under Investigation by firm

Action

On 7/30/21, CardioQuip, issued a "Urgent Medical Device Correction" notification to affected consignees. The notification was provided online through CardioQuip's website and mailed letters. In addition to notifying consignees about the recall, the firm requested consignees take the following actions to reduce the risk of patient infection: 1. The optional Airflow Redirection Hood (MCH-10ARH) may be installed onto the Refrigeration Module(MCH-10RMS) as a potential mitigant to aerosolization. This device is attached overtop the Refrigeration Module and directs exhaust downwards, thereby redirecting potential aerosols downwards and away from the surgical field. Refer to the MCH Operator/Service Manual R3 2021 for installation instructions. Contact your local CardioQuip representative for assistance purchasing the optional Airflow Redirection Hood for your Refrigeration Module. 2.Ensure all modules and accessories, including the Airflow Redirection Hood and Refrigeration Module,are cleaned and disinfected at the same time as the MCH unit according to the Maintenance section on pg. 47 of the MCH Operator/Service Manual R3 2021. 3.Do NOT move modules or accessories between cooler-heater devices to prevent possible cross-contamination. 4.Please forward this notice to all device users and other parties within and outside your organizationthat need to be aware of this correction. 5. CardioQuip continues to develop a more comprehensive understanding of these risks and determine further action. If you have any questions or concerns regarding the Refrigeration Module (MCH-10RMS), optional Airflow Redirection Hood (MCH-10ARH), or proper device maintenance procedures, please contact CardioQuip via phone or email at: CardioQuip Customer Service: +1 (979) 691-0202 Monday Friday 8 A.M. 5 P.M. CT service@cardioquip.com 6. Receipt and understanding of the corrective action outlined in this letter is required from each CardioQuip customer. Please complete and return the e

Quantity

1380 units

Distribution

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.

Lot, serial or model codes

All Serial Numbers

510(k) numbers

["K102147"]

PMA numbers

not on file

Product code

DWC

Firm FEI

3007899424

Firm city

College Station

Firm state

TX

Firm country

not on file

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

Copy