CardioQuip, LLC recalls
Every recall we track for CardioQuip, LLC — 9 in all, from 2021–2023 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from CardioQuip, LLC peaked in 2021 (5); 9 since 2017. 11% rated “stop using now”.
All FDA recall records for CardioQuip, LLC since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 1 | 0 | 4 | 0 | 5 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 1 | 2 | 1 | 4 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled CardioQuip, LLC product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All CardioQuip, LLC recalls
4 shown- Lower riskMedical device
CardioQuip, LLC recalls CardioQuip Modular Cooler-Heater, Model: MCH-1000(m), Power: 115V-60Hz, 16A
CardioQuip recalls MCH-1000(m) modular cooler-heaters due to potential bacterial contamination causing patient infections. Affected units have specific UDI and lot numbers.
CardioQuipOct 24, 2023 - Use cautionMedical device
CardioQuip, LLC recalls CardioQuip Modular Cooler-Heater, Model:MCH-1000(i), Power: 115V-60hz,16A
CardioQuip recalls MCH-1000(i) cooler-heaters with potential heating chamber melting/burning. Affected units have specific serial numbers. Stop using immediately to prevent fire or injury.
CardioQuipOct 19, 2023 - Stop using nowMedical device
CardioQuip, LLC recalls CardioQuip, Modular Cooler-Heater 1000(i), Refrigeration Module, Model: MCH-10RMS, UDI: (01)00860000846127 used with
CardioQuip recalls MCH-10RMS refrigeration modules used in surgery due to potential bacterial growth in water systems that could infect patients during procedures.
CardioQuipJun 24, 2021 - Lower riskMedical device
CardioQuip, LLC recalls CardioQuip, Modular Cooler-Heater, Model: MCH-1000(i), CE 2797, UDI: (01)00860000846103
CardioQuip recalls MCH-1000(i) modular cooler-heaters due to missing water quality maintenance instructions. Owners should check serial numbers and contact for guidance.
CardioQuipMay 12, 2021
CardioQuip, LLC recall questions
How many recalls has CardioQuip, LLC had?
9 recalls from CardioQuip, LLC are on record with U.S. safety agencies, from 2021–2023.
What is the most recent CardioQuip, LLC recall?
CardioQuip, LLC recalls CardioQuip Modular Cooler-Heater, Model: MCH-1000(m), Power: 115V-60Hz, 16A, dated Oct 24, 2023. Every CardioQuip, LLC recall is listed on this page, newest first.
What should I do if I have a recalled CardioQuip, LLC product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new CardioQuip, LLC recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.