MEERA CL mobile operating table 700001B0Recalls & reported problems
MAQUET GmbH · Class 1
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 04046768136786), received between Jun 27, 2024 and Jun 27, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Unintended Movement” (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-0462-2025 · Root cause: Component design/selection · FDA record ↗
Most reported problems
Device problems
- Unintended Movement1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 27, 2024Unintended Movement; Unintended Movement
ON 28TH MAY 2024, GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR MOBILE TABLES - 700001B0 - MEERA CL MOBILE OPERATING TABLE EU. AS IT WAS STATED, THE TABLE TOP MOVED BY ITSELF TO TILTING POSITION WHEN THE PATIENT WAS ON THE TABLE. BASED ON THE INFORMATION PROVIDED, THE TABLE WAS TESTED BY ADDING SOME WEIGHT ON THE SIDE OF THE TABLE TOP AND IT SUDDENLY MOVED. THE SAME THING WAS TESTED ON ANOTHER TABLE BUT IT DID NOT MOVE. ADDITIONALLY, THE BASE OF TABLE WAS ALSO CHECKED. NO LEAKS OF HYDRAULIC OIL WERE FOUND AND IT WAS CONFIRMED THAT THERE WAS ENOUGH OIL IN THE TANK. ACCORDING TO PROVIDED ALLEGATION, THE ISSUE DOES NOT ALWAYS OCCUR. SOMETIMES, WHEN THE TABLE TOP IS MOVED TO TILTING POSITION THE TABLE STAYS IN PLACE. HOWEVER, WHEN CERTAIN POINT IS REACHED THE TABLE CAN BE MOVED WITH SOME WEIGHT. THERE WAS NO INJURY REPORTED, HOWEVER, WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATION, NAMELY THE UNINTENDED MOTION WITH THE PATIENT ON TABLE TOP, WAS TO REOCCUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19623916 ↗
Other TABLE, OPERATING-ROOM, AC-POWERED devices
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- 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.