CardioQuip Modular Cooler-Heater, Model:MCH-1000(i), Power:… recallZ-0439-2024 · CardioQuip, LLC · initiated Oct 19, 2023
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from CardioQuip, LLC or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
There is a potential for the heating-chamber to malfunction resulting in melting/burning of the heater chamber components.
FDA root cause category: Device Design
What the company is doing
On 10/19/23, CardioQuip issued a "Urgent: Medical Device Correction" notification to all affected consignees. This notification was an update to the firm's May 22, 2023 communication. CardioQuip ask consignees to take the following actions: 1. Prime the MCH-1000(i) and MCH-1000(m) prior to each use. 2.Never operate the device dry (see communication for further details). 3. Design Changes to be implemented (see communication for further details). A. Relocation of the water Level Sensor (see communication for further details). B. Software Update (see communication for further details). 4. Please fill out and submit the receipt of understanding of the contents of this letter to CardioQuip within 5 business days or receipt. 5. Any adverse events experienced relating to CardioQuip devices should be reported to CardioQuip or through the FDA s MedWatch Program: Phone: +1 (800) FDA-1088 Web: www.fda.gov/medwatch/report.htm
Recall details
- Recall number
- Z-0439-2024
- Status
- Open, Classified
- Initiated by the company
- Oct 19, 2023
- Posted by the FDA
- Dec 1, 2023
- Recalling firm
- CardioQuip, LLC
- Quantity
- 125 units
- Product code
- DWC
- FDA submissions
- K102147
- Distribution
- US Distribution: TX, IN, IL, WI, FL, NJ, PA, KY, VA, WV, CT, CA, WA, AL, IA
Product description
CardioQuip Modular Cooler-Heater, Model:MCH-1000(i), Power: 115V-60hz,16A
Code information (models, lots, serial numbers)
Show the full code information (1k characters)
UDI: (01)00860000846103/ Serial Numbers: Serial Numbers: 10160461, 10160463, 10160465, 10160466, 101060467, 10160468, 10161406, 10161408, 10161553, 10161689, 10160275 1016276, 1016277, 10160274, 10161065, 10161066, 10160825, 10160826, 10160827, 10160828, 10161140, 10161141, 10160830, 10160831, 10160832, 10160833, 10161543, 10160449, 10160450, 10160451, 10160452 , 1016050512, 10160513, 10160781, 10160785, 10160786, 10160787, 10160788, 10160789, 10160790, 10160791, 10160792, 10160793, 10160794, 10160795, 10161130, 10161131, 10161329, 10161517, 10160758, 10160094, 10160095, 10160096, 10160110, 10160113, 10160114, 10161294, 10161301, 10161303, 10161304, 10161306, 10160570, 10160572, 10160623 ,10160797, 10160798, 10160279, 10160280, 10160281, 10160282, 10161021, 10160797, 10161199, 10161200, 10161275, 10161343, 10161344, 10161560, 10161561, 10160824, 10160767, 10160097, 10160098, 10160099, 10160104, 10160105, 10160106, 10160108, 10160109, 10161043, 10161187, 10161679, 10161680, 10161681, 10160983, 10161830, 10160517, 10160519, 10160520, 10161312, 10160190, 10160191, 10160192, 10160193, 10160194, 10160248, 10160249, 10160250, 10160251, 10160967, 10160683, 10160684, 10160685, 10160686, 10160687, 10160688, 10160689, 10160690, 10161358, 10161359, 10161362, 10160084, 10160161, 10160183, 10161841
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- CardioQuip Modular Cooler-Heater (MCH) MCH-1000(i)Cardioquip, LLC · Controller, Temperature, Cardiopulmonary Bypass2 recalls334 reports
Other devices under the same FDA submission
1 device cleared under K102147 are not named by identifier in this recall. One submission often covers many models, so they may or may not be affected.
- CardioQuip Modular Cooler-Heater (MCH) MCH-1000(m)Cardioquip, LLC · Controller, Temperature, Cardiopulmonary Bypass2 recalls206 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 93347).
- Z-0438-2024 · Open, ClassifiedCardioQuip Modular Cooler-Heater, Model:MCH-1000(m), Power: 115V-60hz,16A
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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