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NA MST-VRecalls & reported problems

Belimed AG · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07640141626153), received between Sep 14, 2024 and Sep 14, 2024 — classified as 1 injury.

The most frequently reported specific device problem is “Failure to Align” (1 report).

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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 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: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Failure to Align1

Patient problems

  • Muscle/Tendon Damage1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjurySep 14, 2024Failure to Align; Failure to Align

    THE SPD MANAGER REPORTED THAT AN EMPLOYEE'S SHOULDER WAS INJURED WHILE TRYING TO LIFT A STERILIZER RACK FROM THE CHAMBER ONTO THE TRANSPORT CART. THE EMPLOYEE WENT TO THE EMERGENCY DEPARTMENT TO GET CHECKED OUT BUT WAS NOT HOSPITALIZED. AS OF (B)(6) 2024 THE EMPLOYEE HAS NOT RETURNED TO WORK AND IS NOT ABLE TO DRIVE NOR TO LIFT THEIR ARM. THE INCIDENT IS BEING HANDLED BY THE FACILITY'S OCCUPATIONAL CARE AND THE INJURED INDIVIDUAL IS CURRENTLY AWAITING AN MRI.

    Patient problems: Muscle/Tendon Damage

    MAUDE report 20219482 ↗

Other Sterilizer, Steam devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.