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inCourage® ICS-1M-US-BRecalls & reported problems

Respiratory Technologies, Inc. · Pulsating Therapy Unit · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00841561102808), received between Dec 16, 2019 and Dec 16, 2019 — classified as 1 injury.

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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Patient Problem/Medical Problem1

Recent adverse event reports

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

  • InjuryDec 16, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    THE MANUFACTURER RECEIVED INFORMATION ALLEGING A PATIENT WAS ADMITTED TO THE HOSPITAL FOR FRACTURED RIBS. THE DEVICE WAS RETURNED TO THE MANUFACTURER FOR EVALUATION AND THE CUSTOMER'S COMPLAINT COULD NOT BE DUPLICATED. THE DEVICE WAS FOUND TO OPERATE AS DESIGNED AND PASSED ALL TESTING. DURING EVALUATION, THE DEVICE WAS FOUND TO HAVE LIQUID INGRESS. THE DEVICE WAS SCRAPPED.

    Patient problems: Patient Problem/Medical Problem

    MAUDE report 9476336 ↗

Other Percussor, Powered-Electric devices

All Percussor, Powered-Electric devices →

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