Recall Z-2420-2025— MAQUET GMBH
Class II · Ongoing
Class II FDA medical device recall by MAQUET GMBH, initiated 2025-07-14. FDA's recall record names no specific 510(k) clearance for this event. Product: Corin Operating Tables Model Numbers: (1) 770001A0, (2) 770001A2, (3) 770001B0, (4) 770001B2, (5) 770001F0, (6) 770001F2; All Software Versions.. 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..
- Recalling firm
- MAQUET GMBH
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-07-14
- Firm location
- Rastatt, Germany
Product description
Corin Operating Tables Model Numbers: (1) 770001A0, (2) 770001A2, (3) 770001B0, (4) 770001B2, (5) 770001F0, (6) 770001F2; All Software Versions.
Reason for recall
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.