Smartview Hotspot LandlineRecalls & reported problems
Microport Crm Srl · Class 3
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 08031527014630), received between Feb 1, 2018 and Feb 1, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Operates Differently Than Expected” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Device Operates Differently Than Expected1
- No Apparent Adverse Event1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 1, 2018Device Operates Differently Than Expected; No Apparent Adverse Event; Device Operates Differently Than Expected; No Apparent Adverse Event
IT WAS REPORTED THAT WHEN THE CLINIC ATTEMPTED TRANSMISSION WITH EQUIPMENT, THE CLINIC DETERMINED THE EQUIPMENT WAS NOT OPERATIONAL. THE CLINIC REPORTED "THIS PRODUCT DOES NOT "PAIR" WITH A PATIENT'S MONITOR AS IT IS A KA860 UNIT".
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7233612 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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