FDA Device recall Z-2420-2025

Corin Operating Tables Model Numbers: (1) 770001A0, (2) 770001A2, (3) 770001B0, (4) 770001B2, (5) 770001F0, (6) 770001F2

FDA Device
Class II
ongoing
Published 2025-09-03

On 2025-09-03 the FDA classified a Class II recall of Corin Operating Tables Model Numbers: (1) 770001A0, (2) 770001A2, (3) 770001B0, (4) 770001B2, (5) 770001F0, (6) 770001F2 by Maquet, citing 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….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-2420-2025
Classification	Class II
Status	ongoing
Initiated	2025-07-14
Published	2025-09-03
Last updated	2026-09-13 11:57 UTC
Company	Maquet
Distribution	US

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.

Identifiers

code_info	Model Numbers: (1) 770001A0, (2) 770001A2, (3) 770001B0, (4) 770001B2, (5) 770001F0, (6) 770001F2; UDI-DI: (1) 04046768… 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, 22, 4, 5, 6, 7, 8, 9, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 24, (2) 9, 51, 53, 14, 15, 16, 17, 34, 35, 36, 37, 39, 40, 42, 43, 54, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 38, 44, 45, 46, 5, 13, 57, 58, 59, 18, 49, 47, 48, 7, 52, (3) 41, 5, 6, 45, 48, 49, 50, 23, 38, 10, 12, 13, 14, 84, 87, 88, 89, 7, 63, 80, 82, 83, 86, 54, 93, 94, 11, 15, 18, 20, 21, 22, 27, 28, 32, 40, 9, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 85, 55, 56, 57, 58, 59, 42, 97, 92, 17, 26, 16, 24, 25, 30, 33, 35, 36, 37, 39, 44, 53, 91, 8, 19, 90, 46, 47, 51, 52, 34, 43, 60, 62, 64, 65, 66, 67, 68, (4) 44, 70, 71, 42, 56, 65, 115, 185, 52, 105, 106, 107, 109, 145, 146, 147, 148, 11, 26

code_info

Model Numbers: (1) 770001A0, (2) 770001A2, (3) 770001B0, (4) 770001B2, (5) 770001F0, (6) 770001F2; UDI-DI: (1) 04046768…

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, 22, 4, 5, 6, 7, 8, 9, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 24, (2) 9, 51, 53, 14, 15, 16, 17, 34, 35, 36, 37, 39, 40, 42, 43, 54, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 38, 44, 45, 46, 5, 13, 57, 58, 59, 18, 49, 47, 48, 7, 52, (3) 41, 5, 6, 45, 48, 49, 50, 23, 38, 10, 12, 13, 14, 84, 87, 88, 89, 7, 63, 80, 82, 83, 86, 54, 93, 94, 11, 15, 18, 20, 21, 22, 27, 28, 32, 40, 9, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 85, 55, 56, 57, 58, 59, 42, 97, 92, 17, 26, 16, 24, 25, 30, 33, 35, 36, 37, 39, 44, 53, 91, 8, 19, 90, 46, 47, 51, 52, 34, 43, 60, 62, 64, 65, 66, 67, 68, (4) 44, 70, 71, 42, 56, 65, 115, 185, 52, 105, 106, 107, 109, 145, 146, 147, 148, 11, 26

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2420-2025%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.