Fairfield, NJ, United States
Maquet recalls
2 recalls recorded since 2018, most recently on 14 July 2025. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls2
Ongoing (FDA)1
Terminated or completed1
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 14 July 2025
- Reason
- Under certain conditions, such as the simultaneous use of the operating table with other medical devices, including high-frequency (HF) surgical equipment, interference may occur that could prevent the device from performing as intended. If the issue occurs, the operating table is unresponsive to command from both the universal remote control and override panel.
- Distribution
- Worldwide - US Nationwide distribution in the states of KY, NY, TX and the countries of Algeria, Australia, Austria, Bulgaria, Canada, China, Colombia, Denmark, Egypt, Estonia, Finland, France, Germany, Ireland, Israel, Italy, Japan, Jordan, Korea, Republic of, Kuwait, Lebanon, Morocco, Netherlands
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2420-2025
- Corin Operating Tables Model Numbers: (1) 770001A0, (2) 770001A2, (3) 770001B0, (4) 770001B2, (5) 770001F0, (6) 770001F2; All Software Versions.
Terminated Class II Medical devices
- Recall started
- 22 May 2017
- Terminated
- 12 July 2018
- Reason
- 55 kits were distributed after their expiration date of September 2015.
- Distribution
- Distributed to the states of NM, CA, and IL.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0490-2018
- Hemofiltration Standard Pack including BC 60 Plus-T 8036. Part Number: 701066990. Used in extracorporeal circulation during cardiopulmonary bypass procedures lasting 6 hours or less.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.