Tempus Pro 01-2051Recalls & reported problems
Remote Diagnostic Technologies Limited · Tempus Lithium-Ion Battery (Black) · 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 05060472440297), received between Jun 16, 2022 and Jun 16, 2022 — 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.
Most reported problems
Device problems
- Insufficient Device Problem Information1
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.
MalfunctionJun 16, 2022Insufficient Device Problem Information; Insufficient Device Problem Information
AS DESCRIBED BY THE CUSTOMER "TEMPUS IC LI-ION BATTERY EXPLODED WHILE BEING CHARGED BY TEMPUS BATTERY CHARGER". INITIAL EVALUATION BASED ON THE CUSTOMER COMMUNICATIONS REVEAL THAT TEMPUS IC PRO, THE AFFECTED PRODUCT BUILT & SHIPPED TO OUR CUSTOMER, US SOCOM (US SPECIAL FORCES), BACK IN 2011. ADVENTURE MEDICS, WHO REPORTED THIS COMPLAINT, PURCHASED EITHER FROM GOVT AUCTION OR FROM EBAY. THERE IS NO FURTHER EVALUATION POSSIBLE FOR THIS CASE SINCE CUSTOMER DISPOSED THE BATTERY DEBRIS AND THE PRODUCT IS END OF LIFE. CAUSE COULD NOT BE DETERMINED. CUSTOMER HAS BEEN INFORMED ABOUT PRODUCT END OF LIFE AND NO SUPPORT FROM PHILIPS FOR THE PARTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14716134 ↗
Other Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) devices
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.