Provider 790Recalls & reported problems
Jeron Electronic Systems, Inc. · 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 00860002736020), received between Dec 31, 2025 and Dec 31, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Self-Activation or Keying” (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
- Self-Activation or Keying1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 31, 2025Self-Activation or Keying; Self-Activation or Keying
ON DEC. 4, 2025, MEDWATCH FORM WAS FORWARDED FROM FDA TO THE COMPANY. MEDWATCH FORM WAS SUBMITTED ANONYMOUSLY AND REPORTED A CODE BLUE NOTIFICATION WHEN THE PATIENT DID NOT ACTIVATE THE CALL BUTTON.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23933874 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.