Vios 310F83-LC+Recalls & reported problems
Pari Respiratory Equipment, Inc. · Vios Nebulizer System, LC Plus · 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 00744229310679), received between Nov 6, 2020 and Nov 6, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Sparking” (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
- Sparking1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 6, 2020Sparking; Sparking
ELECTRICAL EVENT [DEVICE ELECTRICAL FINDING]. ON (B)(6) 2020, A SPONTANEOUS REPORT WAS RECEIVED FROM A CONSUMER REGARDING A (B)(6) YEAR-OLD FEMALE PATIENT'S EXPERIENCE WITH VIOS (NEBULIZER). THE PATIENT WAS NOTED TO BLIND AND IN A WHEELCHAIR. ON (B)(6) 2020, THE CONSUMER STATED THAT WHEN HER PHYSICAL THERAPIST PLUGGED THE COMPRESSOR POWER CORD INTO THE WALL OUTLET, THEY SAW FLAMES COME OUT OF THE OUTLET. NEITHER PATIENT NOR THERAPIST WERE INJURED ACCORDING TO THE THERAPIST.
Patient problems: Insufficient Information
MAUDE report 10805066 ↗
Other Nebulizer (Direct Patient Interface) devices
- HUDSON RCI IPN049807Teleflex Incorporated · NEBULIZER (DIRECT PATIENT INTERFACE)62 reports
- Circulaire™ 0330Sunmed, LLC · Nebulizer (Direct Patient Interface)1 recall0 reports
- I neb 00Respironics Respiratory Drug Delivery (Uk) Ltd · NEBULIZER (DIRECT PATIENT INTERFACE)3 deaths15 reports
- VixOne 0209Westmed, Inc. · Nebulizer (Direct Patient Interface)13 reports
- HUDSON RCI IPN040620Teleflex Incorporated · NEBULIZER (DIRECT PATIENT INTERFACE)12 reports
- HUDSON RCI IPN049808Teleflex Incorporated · NEBULIZER (DIRECT PATIENT INTERFACE)6 reports
- HUDSON RCI HUD05014Medline Industries, Inc. · Nebulizer (direct patient interface)6 reports
- VixOne 0210Westmed, Inc. · Nebulizer (Direct Patient Interface)5 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.
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