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Site-Rite 9770176RRecalls & reported problems

Bard Access Systems, Inc. · REFURB, SR VISION II DISPLAY · 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 00801741125355), received between Oct 8, 2021 and Oct 8, 2021 — classified as 1 malfunction.

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

  • No Apparent Adverse Event1

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.

  • MalfunctionOct 8, 2021No Apparent Adverse Event; No Apparent Adverse Event

    THE INSULATION ON THE CORD IS ALL COMING OFF EXPOSING WIRING.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12599027 ↗

Other System, imaging, pulsed echo, ultrasonic devices

All System, imaging, pulsed echo, ultrasonic devices →

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