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Philips DreamStationRecalls & reported problems across all models

Respironics, Inc. · 190 models in the FDA device registry

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
32,422
Deaths reported
484
Injuries reported
5,864
Recalls
0

We found 190 models of Philips DreamStation by Respironics, Inc. in the FDA's device registry (GUDID). Together they are named in 32,422 adverse event reports in the FDA's MAUDE database, received between Sep 28, 2016 and Sep 30, 2026 — classified as 484 deaths, 5,864 injuries, 26,074 malfunctions.

The most frequently reported specific device problem is “Degraded” (31,854 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Reports received per month, all models

Nov 2023: 160 reportsDec 2023: 122 reportsJan 2024: 152 reportsFeb 2024: 206 reportsMar 2024: 215 reportsApr 2024: 242 reportsMay 2024: 290 reportsJun 2024: 244 reportsJul 2024: 453 reportsAug 2024: 2,046 reportsSep 2024: 2,262 reportsOct 2024: 1,308 reportsNov 2024: 1,254 reportsDec 2024: 812 reportsJan 2025: 1,135 reportsFeb 2025: 3,866 reportsMar 2025: 5,223 reportsApr 2025: 516 reportsMay 2025: 305 reportsJun 2025: 354 reportsJul 2025: 182 reportsAug 2025: 91 reportsSep 2025: 80 reportsOct 2025: 93 reportsNov 2025: 480 reportsDec 2025: 64 reportsJan 2026: 37 reportsFeb 2026: 780 reportsMar 2026: 123 reportsApr 2026: 51 reportsMay 2026: 1,431 reportsJun 2026: 2,489 reportsJul 2026: 4 reportsAug 2026: 4 reportsSep 2026: 13 reportsOct 2026: 0 reports2024202520265,223
Last 36 months. The most recent month may be incomplete.

Most reported Philips DreamStation problems

Device problems

  • Degraded31,854
  • Contamination557
  • Adverse Event Without Identified Device or Use Problem348
  • Corroded124
  • No Apparent Adverse Event56
  • Material Integrity Problem41
  • Insufficient Device Problem Information40
  • Overheating of Device35

Patient problems

  • No Clinical Signs, Symptoms or Conditions23,502
  • Unspecified Respiratory Problem4,248
  • Headache2,684
  • Dizziness2,362
  • Cancer2,078
  • Asthma1,625
  • Unspecified Kidney or Urinary Problem1,501
  • Eye Irritation1,266

Philips DreamStation models

190 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.

Recent Philips DreamStation adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

Other Respironics, Inc. products

All Respironics, Inc. devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page