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MAGNUS operating table systemRecalls & reported problems across all models

MAQUET GmbH · 8 models in the FDA device registry

Data updated Oct 16, 2026 from official FDA records · Editorial policy

1 open recall names at least one MAGNUS operating table system model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.

Adverse event reports
39
Deaths reported
0
Injuries reported
0
Recalls
1

We found 8 models of MAGNUS operating table system by MAQUET GmbH in the FDA's device registry (GUDID). Together they are named in 39 adverse event reports in the FDA's MAUDE database, received between Mar 16, 2023 and Apr 24, 2026 — classified as 39 malfunctions.

The most frequently reported specific device problem is “Positioning Failure” (20 reports).

1 FDA recall record name at least one of these models by its device 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. 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

Nov 2023: 3 reportsDec 2023: 5 reportsJan 2024: 4 reportsFeb 2024: 2 reportsMar 2024: 2 reportsApr 2024: 2 reportsMay 2024: 0 reportsJun 2024: 1 reportsJul 2024: 0 reportsAug 2024: 2 reportsSep 2024: 1 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 1 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 1 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 3 reportsApr 2026: 2 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520265
Last 36 months. The most recent month may be incomplete.

MAGNUS operating table system 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. Feb 11, 2021Open, Classified

    There is a potential for hydraulic leakage at the inclination function to occur resulting in an unintended Trendelenburg or anti-Trendelenburg movement of the table top depending on patient positioning which may lead to the patient having to be transferred to another OR table causing a delay in the procedure.

    Z-1296-2021 · Root cause: Device Design · names 8 of these models · Recall details · FDA record ↗

Most reported MAGNUS operating table system problems

Device problems

  • Positioning Failure20
  • Communication or Transmission Problem9
  • Computer Software Problem6
  • Use of Device Problem6
  • Degraded5
  • Device Sensing Problem5
  • Failure to Sense5
  • Positioning Problem4

Patient problems

  • No Clinical Signs, Symptoms or Conditions39

MAGNUS operating table system models

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

Recent MAGNUS operating table system adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

Other MAQUET GmbH products

All MAQUET GmbH devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page