Life Support Products L760CPAPRecalls & reported problems
Allied Medical, LLC · Autovent 4000 with CPAP · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00026072001349), received between Jun 7, 2022 and Oct 1, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Energy Output 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. 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
- Energy Output Problem1
- Failure to Deliver1
- Insufficient Device Problem Information1
- Therapeutic or Diagnostic Output Failure1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Insufficient Information1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 1, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
CUSTOMER REPORTED THE THE UNIT WAS NOT CYCLING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20348279 ↗MalfunctionJun 7, 2022Energy Output Problem
THE AUTOVENT 4000 WITH CPAP WAS CHECKED PRIOR TO PUTTING INTO SERVICE. IT WAS FOUND THAT THE UNIT FAILED TO DELIVER A BREATH BUT DID FUNCTION ONCE THE MANUAL BREATH BUTTON WAS ACTIVATED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14626930 ↗MalfunctionJun 7, 2022Failure to Deliver; Therapeutic or Diagnostic Output Failure
THE AUTOVENT 4000 WITH CPAP WAS CHECKED PRIOR TO PUTTING INTO SERVICE. IT WAS FOUND THAT THE UNIT FAILED TO DELIVER A BREATH BUT DID FUNCTION ONCE THE MANUAL BREATH BUTTON WAS ACTIVATED.
Patient problems: Insufficient Information
MAUDE report 14626806 ↗
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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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