MAQUET (Suzhou) Co., Ltd
7 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (7)
Registered facilities (1)
- MAQUET (SUZHOU) CO., LTD FEI 3007417753 · CN
Recalls & enforcement
- Class IIOngoing2026-08-07The potential for the device to detach at the junction between the spring arm and suspension arm and fall causing potential injury.
- Class IIOngoing2025-07-14Under 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 i…
- Class IITerminated2018-06-14Certain VOLISTA StandOP Surgical Lights have been identified as having a potential light head detachment issue. Improper assembly of the bracket that connects the light head to the axle fork could result in the light head bracket breaking, causing the light head to detach from th…
- Class IITerminated2018-04-19Potential keypad failure on VOLISTA StandOP Surgical Lights.
- Class IITerminated2017-05-2255 kits were distributed after their expiration date of September 2015.
- Class IITerminated2012-11-02There is a potential issue with the screw tension of the extension device 1433.62A1 used with the YUNO table.
- Class IITerminated2012-05-29Certain pediatric arterial cannulas may have limited flexibility due to an increased length of the "hardened" cannula tip.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “MAQUET (Suzhou) Co., Ltd — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-10027696-maquet-suzhou-co-ltd/
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