NIBP Cuffs EASY CARE CUFF, 1 HOSE, ADULT XL (1)Recalls & reported problems
Philips Medical Systems Hsg · Antimicrobial NIBP Cuff, Reusable, Single Hose, Adult X-Long (1) · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 1
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00884838003125), received between Jun 27, 2022 and Jun 27, 2022 — classified as 1 death.
The most frequently reported specific device problem is “Incorrect, Inadequate or Imprecise Result or 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.
Most reported problems
Device problems
- Incorrect, Inadequate or Imprecise Result or Readings1
Patient problems
- Low Blood Pressure/ Hypotension1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
DeathJun 27, 2022Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED TO PHILIPS THAT THE A PATIENT DIED DUE TO BLOOD PRESSURE MONITOR FAILURE. THE DEVICE WAS IN USE AT TIME OF EVENT AND PATIENT DIED.
Patient problems: Low Blood Pressure/ Hypotension
MAUDE report 14827988 ↗
Other Antimicrobial blood pressure cuff devices
- NIBP Cuffs EASY CARE CUFF, 1 HOSE, ADULT (1)Philips Medical Systems Hsg · Antimicrobial blood pressure cuff4 reports
- NIBP Cuffs Single Care Cuff, AdultPhilips Medical Systems Hsg · Antimicrobial blood pressure cuff1 report
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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