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PHILIPS 1076374Recalls & reported problems

Respironics California, Inc. · Assy Battery Li-Ion,11ah,V60 · 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 00884838020429), received between Apr 9, 2020 and Apr 9, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “No Display/Image” (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

  • No Display/Image1

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.

  • MalfunctionApr 9, 2020No Display/Image

    THE CUSTOMER REPORTED BATTERY ORDERED, DID NOT DISPLAY THE MANUFACTURE DATE IN THE PNEUMATICS SCREEN. THE UNIT WAS IN CLINICAL USE AT THE TIME THE REPORTED ISSUE WAS DISCOVERED. HOWEVER, THERE WAS NO PATIENT HARM REPORTED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9947070 ↗

Other Ventilator, continuous, minimal ventilatory support, facility use devices

All Ventilator, continuous, minimal ventilatory support, facility use devices →

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