MEERA ST mobile operating table 710001B0Recalls & reported problems
MAQUET GmbH · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04046768136298), received between Oct 10, 2023 and Oct 10, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Recalls naming this device
- Oct 3, 2024Open, Classified
Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay
Z-0460-2025 · Root cause: Component design/selection · FDA record ↗
Most reported problems
Device problems
- Insufficient Device Problem Information1
- Use of Device Problem1
Patient problems
- Unspecified Tissue Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 10, 2023Use of Device Problem; Insufficient Device Problem Information; Use of Device Problem; Insufficient Device Problem Information
ON 2ND OCTOBER 2023 GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR MOBILE TABLES - 710001B0 - MEERA ST EU WITHOUT AUTO DRIVE. AS IT WAS STATED, THE FOLLOWING COURSE OF EVENTS OCCURRED. THE DOCTOR WAS ON THE RIGHT SIDE OF THE DEVICE. THE TABLE WAS IN THE TRENDELENBURG POSITION TITLED TO THE RIGHT. AFTER REPOSITIONING THE TABLE INTO ZERO POSITION BY PERFORMING THE DOWNWARD MOVEMENT, THE DOCTOR'S FOOT WAS PRESSED LATERALLY BY THE BASE OF THE TABLE LEADING TO SKIN INJURY OF THE USER. ACCORDING TO THE PROVIDED INFORMATION, THE INCIDENT DID NOT RESULT IN ANY MAJOR INJURY. ADDITIONAL DETAILS OF THE EVENT AND USER'S OUTCOME WERE REQUESTED, HOWEVER, NO INFORMATION HAS BEEN RECEIVED TO DATE. IT WAS CONFIRMED THAT THE PATIENT WAS NOT HARMED IN THIS EVENT. WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATION, NAMELY THE USER'S FOOT BEING PRESSED BY THE BASE OF THE TABLE, WAS TO REOCCUR.
Patient problems: Unspecified Tissue Injury
MAUDE report 17903383 ↗
Other TABLE, OPERATING-ROOM, AC-POWERED devices
- ORT300 TableIMRIS Imaging, Inc. · Table, Operating-Room, Ac-Powered2 recalls21 reports
- ORT200 TableIMRIS Imaging, Inc. · Table, Operating-Room, Ac-Powered2 recalls12 reports
- MEERA mobile operating table 720001F2MAQUET GmbH · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- HarmonyAIR A-Series Suspension SystemSteris Corporation · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- HarmonyAIR A-Series Suspension SystemSteris Corporation · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- HarmonyAIR A-Series Suspension SystemSteris Corporation · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- MEERA mobile operating table 720001B2MAQUET GmbH · TABLE, OPERATING-ROOM, AC-POWERED1 recall19 reports
- MAGNUS operating table system 118001B2MAQUET GmbH · TABLE, OPERATING-ROOM, AC-POWERED1 recall17 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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