Grass® MR Conditional/CT Cup Electrodes MRARR27-59Recalls & reported problems
Natus Manufacturing Limited · Grass® MR Conditional/CT Cup Electrodes Array, 27 leads, 3 arrays, 1.5M · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00382830051255), received between Feb 27, 2026 and Feb 27, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- Superficial (First Degree) Burn1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 27, 2026Insufficient Device Problem Information
MRARR27-59 (MR ARRAY D/C ELECTRODE 27 LEAD W/1.5M EXT) - A PATIENT WAS BURNED BY ONE OF THE MR ELECTRODES (OF A 27-ARRAY). THEY WERE USING THIS PARTICULAR ELECTRODE AS AN EKG ON THE PATIENT'S SHOULDER AND IT BURNED THE PATIENT. IT WAS CONFIRMED THAT THE PATIENT DID NOT EXPERIENCE ANY OTHER BURNS FROM ANY OTHER ELECTRODES.
Patient problems: Superficial (First Degree) Burn
MAUDE report 24474681 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.