Invacare® Perfecto2™ Oxygen Concentrator IRC5PO2VRecalls & reported problems
Invacare Corporation · Class 2
All models of Invacare Perfecto2 Oxygen Concentrator (2)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00841447100010), received between Dec 7, 2018 and Mar 4, 2025 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Explosion” (2 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, 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
- Explosion2
- Fire1
- Material Deformation1
- Material Discolored1
- Overheating of Device1
- Smoking1
Patient problems
- No Consequences Or Impact To Patient3
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 4, 2025Fire; Fire
IT WAS REPORTED TO VENTEC THAT AN INVACARE PERFECTO2 OXYGEN CONCENTRATOR ALLEGEDLY CAUGHT FIRE INSIDE A PATIENT'S RESIDENCE. THE FIRE DEPARTMENT WAS DISPATCHED AND UPON ENTRY TO THE APARTMENT, OBSERVED THAT THE FIRE WAS ALREADY OUT AND THAT ONLY A LIGHT SMOKE WAS VISIBLE. THE FIRE DEPARTMENT THEN REMOVED THE OXYGEN CONCENTRATOR FROM THE APARTMENT, THROWING IT INTO THE YARD WHERE A DISTRIBUTOR WAS LATER ABLE TO RETRIEVE IT. THERE WAS PATIENT INVOLVEMENT ASSOCIATED WITH THE REPORTED EVENT. THERE WERE NO REPORTS OF PATIENT HARM AS A RESULT OF THE REPORTED ISSUE. THE PATIENT DECLINED MEDICAL TREATMENT AT THE SCENE. NO FURTHER DETAILS WERE PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21521150 ↗MalfunctionMar 18, 2019Material Discolored; Material Deformation; Explosion; Material Discolored; Material Deformation; Explosion
THE REPORTER STATED THE TOP OF THE PRODUCT TANK AND THE PRESSURE REGULATOR HAD COME OFF IN PIECES CAUSING THE CABINET CASING TO BREAK INTO TWO PIECES, AND SIEVE DUST WAS THROUGHOUT THE UNIT. THE END USER WAS NOT IN THE ROOM AT THE TIME, AND NO INJURY WAS ALLEGED. THE UNIT WAS A RENTAL UNIT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8429229 ↗MalfunctionJan 24, 2019Overheating of Device; Explosion; Overheating of Device; Explosion
THE PROVIDER REPORTED THAT THE IRC5PO2V CONCENTRATOR MADE A LOUD NOISE, AND IT WAS DISCOVERED THAT THE PRODUCT TANK SEAL HAD BURST AND PUNCTURED THROUGH THE TOP SHROUD, WHICH DAMAGED THE HOUR METER AND SOUND BOX. HE ALLEGED THAT THE METAL CASING OF THE PRODUCT TANK CAP SHOT THROUGH THE TOP SHROUD, SENDING SHARP METAL INTO THE ROOM. THE PROVIDER ADVISED THAT THE UNIT IS A RENTAL AND WAS IN A PATIENT'S HOME WHEN THE INCIDENT OCCURRED, BUT NO INJURIES OR PROPERTY DAMAGE RESULTED FROM THE EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8273945 ↗MalfunctionDec 7, 2018Smoking; Smoking
A REPAIR CENTER TECHNICIAN REPORTED THAT THE PROVIDER SENT THE IRC5PO2V CONCENTRATOR TO THEM, STATING THAT THERE WAS SMOKE COMING FROM THE UNIT. THE REPAIR TECHNICIAN ADVISED THAT WHEN HE TOOK OFF THE CABINET FILTER DOOR, THERE WAS A HOLE IN THE PLASTIC THAT WAS MELTED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8141653 ↗
Other Generator, Oxygen, Portable devices
- DeVilbiss 525DSDevilbiss Healthcare LLC · Generator, Oxygen, Portable2 recalls14 deaths287 reports
- Inogen One G5 Oxygen Concentrator - Bluetooth 1260 BluetoothInogen, Inc. · Generator, Oxygen, Portable3 deaths235 reports
- EverFlo EverFlo w/O2 Percentage Indicator, 230V, EURespironics, Inc. · Generator, oxygen, portable5 deaths112 reports
- Inogen One G3 Oxygen Concentrator 1050Inogen, Inc. · Generator, Oxygen, Portable2 deaths111 reports
- DeVilbiss 125DDevilbiss Healthcare LLC · Generator, Oxygen, Portable2 recalls1 death3 reports
- EverFlo EVERFLO NON-O2 Percentage Indicator, 120V, US,CARespironics, Inc. · Generator, oxygen, portable19 deaths80 reports
- EverFlo EVERFLO w/Oxygen Percentage Indicator, 120V US, CARespironics, Inc. · Generator, oxygen, portable2 deaths71 reports
- SimplyGo Mini SimplyGo Mini, USRespironics, Inc. · Generator, oxygen, portable1 recall1 death5 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 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.
How reports and recalls are matched · Editorial policy · Report an error on this page