Operating tables recalled because interference can leave them unresponsive to controls
Corin Operating Tables are recalled because interference, such as from high-frequency surgical equipment used at the same time, can leave the table unresponsive to both the remote control and the override panel.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: Rubric level 3 covers risk-of-harm products where injury has not yet been reported; an operating table that stops responding during surgery is a potential harm and no injuries are reported.
Plain-English summary
Corin Operating Tables are being recalled under model numbers 770001A0, 770001A2, 770001B0, 770001B2, 770001F0 and 770001F2, across all software versions. The recall covers 315 units, of which 8 are in the United States, distributed in Kentucky, New York and Texas and in a number of other countries.
Under certain conditions, such as the simultaneous use of the operating table with other medical devices including high-frequency surgical equipment, interference may occur that could prevent the device from performing as intended. If the issue occurs, the operating table is unresponsive to commands from both the universal remote control and the override panel. The FDA classified the action as Class II.
Hospitals operating these tables should follow the manufacturer's instructions, including any guidance on use alongside high-frequency surgical equipment.
The recalled product
- Product
- Corin Operating Tables Model Numbers: (1) 770001A0, (2) 770001A2, (3) 770001B0, (4) 770001B2, (5) 770001F0, (6) 770001F2; All Software Versions.
- Manufacturer
- MAQUET GMBH
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- Model Numbers: (1) 770001A0
- (2) 770001A2
- (3) 770001B0
- (4) 770001B2
- (5) 770001F0
- (6) 770001F2
- UDI-DI: (1) 04046768145177
- (2) 04046768145184
- (3) 04046768145191
- (4) 04046768145207
- (5) 04046768145214
- (6) 04046768145221
- Lot/Serial Numbers: (1) 1
- 2
- 3
- 10
- 25
- 26
- 27
- 28
Distribution
Related recalls
Same hazard · electromagnetic interference
See all →- HighSix foot display cables recalled over inadequate shielding and interference
FDA (Devices) · 2025-10-22
- HighTwelve foot display cables recalled over inadequate shielding and interference
FDA (Devices) · 2025-10-22
- HighMonitor display cables recalled over inadequate shielding and electromagnetic interference
FDA (Devices) · 2025-10-22
- HighOlympus Quest Spectrum 3 Fluorescent Imaging System Recalled for EMC Defect
FDA (Devices) · 2024-11-06
- HighIntelliVue Patient Monitors recalled for electrical grounding defect
FDA (Devices) · 2024-10-02
Similar recalls
- HighMeera Mobile Operating Table May Move Unexpectedly During Surgery
FDA (Devices) · 2023-10-11
- HighTrumpf TITAN Operating Room Table Recalled for Unintended Movement
FDA (Devices) · 2014-11-05
- HighBerchtold Corp. Recalls OPERON D850 Surgical Tables Due to Malfunction
FDA (Devices) · 2013-09-18
- HighSteris Surgical Table Recalled for Potential Unintended Movement
FDA (Devices) · 2012-09-26
- ModerateFDA Recalls MEERA CL Mobile Operating Tables for Unintended Movement Stops
FDA (Devices) · 2024-11-20
- HighDeerfield Imaging Recalls IMRIS ORT200 Operating Room Tables for Drift Risk
FDA (Devices) · 2018-04-04