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AtamA™ System 20609Recalls & reported problems

Monteris Medical Inc · AtamA Patient Board · 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 00816589020229), received between Apr 20, 2021 and Apr 20, 2021 — classified as 1 injury.

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.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Bone Fracture(s)1

Recent adverse event reports

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

  • InjuryApr 20, 2021Adverse Event Without Identified Device or Use Problem

    DURING THE TRANSFER OF THE PATIENT FROM THE ATAMA BOARD TO THE MRI BED, THE MRI TECH BROKE A FINGER WHEN IT WAS IN BETWEEN THE ATAMA BOARD AND THE MRI BED.

    Patient problems: Bone Fracture(s)

    MAUDE report 11693755 ↗

Other Coil, Magnetic Resonance, Specialty devices

All Coil, Magnetic Resonance, Specialty devices →

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