Expression MR Wireless SPO2 Patient module (Gen 3) 1-5 Wireless SpO2 3.0 Module (Networks 1-5)Recalls & reported problems
Philips Ds North America LLC · 3rd-Generation wireless SpO2 module for Expression MRI patient monitors (Networks 1-5). · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 00884838055025), received between Jul 31, 2025 and Jul 31, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “High Readings” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- High Readings1
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.
MalfunctionJul 31, 2025High Readings; High Readings
PHILIPS RECEIVED A COMPLAINT ON A WIRELESS SPO2 PATIENT MODULE (GEN 3) 1-5 INDICATING THAT SPO2 IS GIVING INCORRECT READINGS AND THE CUSTOMER WANTS TO KNOW IF UNIT IS NOT COMPATIBLE WITH CERTAIN TESTING EQUIPMENT; THE READINGS SEEMED TOO HIGH. THE DEVICE WAS NOT IN CLINICAL USE AT THE TIME THE ISSUE WAS DISCOVERED. NO ADVERSE EVENT OR HARM WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22676354 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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