MEERA CL mobile operating tableRecalls & reported problems across all models

We found 2 models of MEERA CL mobile operating table by MAQUET GmbH in the FDA's device registry (GUDID). Together they are named in 1 adverse event report in the FDA's MAUDE database, 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).

2 FDA recall records name at least one of these models by its device identifier, 2 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

MEERA CL mobile operating table recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. 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 · Recall details · FDA record ↗

2. 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-0458-2025 · Root cause: Component design/selection · Recall details · FDA record ↗

Most reported MEERA CL mobile operating table problems

MEERA CL mobile operating table models

2 models, most reported first. Each model has its own page with its reports, recalls and device details.

• MEERA CL mobile operating table 700001B0

  TABLE, OPERATING-ROOM, AC-POWERED
  1 recall1 report
• MEERA CL mobile operating table 700001F0

  TABLE, OPERATING-ROOM, AC-POWERED
  1 recall0 reports

Recent MEERA CL mobile operating table adverse event reports

The 1 most recent reports across all models, 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 MAQUET GmbH products

• MEERA mobile operating table3 models · 32 reports · 4 recalls
• ALPHAMAXX mobile operating table3 models · 8 reports · 3 recalls
• MEERA ST mobile operating table3 models · 1 reports · 3 recalls
• MAGNUS operating table system8 models · 39 reports · 1 recall
• CORIN mobile operating table6 models · 9 reports · 1 recall
• OTESUS operating table system3 models · 20 reports