TELE PACK TP100Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04048551322925), received between Jan 5, 2026 and Jan 5, 2026 — classified as 1 injury.

The most frequently reported specific device problem is “Display or Visual Feedback Problem” (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.

Most reported problems

Recent adverse event reports

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

• InjuryJan 5, 2026Display or Visual Feedback Problem

  IT WAS REPORTED THAT NO LIGHT OUTPUT COMING FROM THE UNIT AND THUS THE VITOM TELESCOPE COULD NOT BE USED. FAILURE OF THE UNIT OCCURRED RIGHT BEFORE AN OUTPATIENT PROCEDURE. THE CASE HAD TO BE POSTPONED. THE PATIENT WAS NOT HARMED. NO NEGATIVE IMPACT IN STATE OF HEALTH REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23960083 ↗