MEERA ST mobile operating tableRecalls & reported problems across all models
MAQUET GmbH · 3 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
3 open recalls name at least one MEERA ST mobile operating table model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 3
We found 3 models of MEERA ST 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 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).
3 FDA recall records name at least one of these models by its device identifier, 3 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
Reports received per month, all models
MEERA ST 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.
- 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-0463-2025 · Root cause: Component design/selection · Recall details · FDA record ↗
- 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-0461-2025 · Root cause: Component design/selection · Recall details · FDA record ↗
- 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 · Recall details · FDA record ↗
Most reported MEERA ST mobile operating table problems
Device problems
- Insufficient Device Problem Information1
- Use of Device Problem1
Patient problems
- Unspecified Tissue Injury1
MEERA ST mobile operating table models
3 models, most reported first. Each model has its own page with its reports, recalls and device details.
- MEERA ST mobile operating table 710001B0TABLE, OPERATING-ROOM, AC-POWERED1 recall1 report
- MEERA ST mobile operating table 710001B2TABLE, OPERATING-ROOM, AC-POWERED1 recall0 reports
- MEERA ST mobile operating table 710001F2TABLE, OPERATING-ROOM, AC-POWERED1 recall0 reports
Recent MEERA ST 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.
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 MAQUET GmbH products
- MEERA mobile operating table3 models · 32 reports · 4 recalls
- ALPHAMAXX mobile operating table3 models · 8 reports · 3 recalls
- MEERA CL mobile operating table2 models · 1 reports · 2 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
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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