Medline HCS4525GRecalls & reported problems
Medline Industries, Inc. · TUBING,OXYGEN,CRUSH RES,25',GREEN,SC · Class 1
Data updated Oct 13, 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 10080196416752), received between Jun 3, 2026 and Jun 3, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Infusion or Flow Problem” (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.
Reports received per month
Most reported problems
Device problems
- Infusion or Flow Problem1
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.
MalfunctionJun 3, 2026Infusion or Flow Problem
IT WAS REPORTED THAT WHEN THE CANNULA IS PLUGGED IN, THE AIR COULD NOT GO IN OR OUT, AND THE ALARM WENT OFF TO SAY THAT IT WAS NOT WORKING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25369436 ↗
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- AirLife SO-1188-0Salter Labs · TUBING, PRESSURE AND ACCESSORIES3 reports
- AirLife 2025G-25Salter Labs · TUBING, PRESSURE AND ACCESSORIES2 reports
- Medline HCS4550GBMedline Industries, Inc. · TUBING, PRESSURE AND ACCESSORIES2 reports
- Flow sensor 155500Hamilton Medical AG · Tubing, Pressure And Accessories2 reports
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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