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CVS GVP110Recalls & reported problems

Woonsocket Prescription Center, Incorporated · CVS Warm Steam Vaporizer · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00050428372609), received between Aug 12, 2021 and Aug 12, 2021 — classified as 1 injury.

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.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Partial thickness (Second Degree) Burn1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryAug 12, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    A CONSUMER STATED SHE RECEIVED SECOND DEGREE BURNS FROM HOT STEAM THAT WAS SPITTING OUT OF THEIR VAPORIZER. IT IS UNKNOWN WHETHER THE WOMAN RECEIVED MEDICAL TREATMENT FOR HER INJURIES. THE INSTRUCTIONS FOR PROPER USE HAVE VERY CLEAR WARNINGS THAT STATE "THE VAPORIZER SHOULD ALWAYS BE PLACED ON A FIRM, FLAT, WATERPROOF SURFACE AT LEAST FOUR FEET AWAY FROM BEDSIDE AND OUT OF REACH OF PATIENTS, CHILDREN, AND PETS", AND "CAUTION: TOO MUCH SALT CAN CAUSE EXCESSIVE BOILING". KAZ USA, INC. HAS REQUESTED THAT THE PRODUCT BE RETURNED FOR TESTING.

    Patient problems: Partial thickness (Second Degree) Burn

    MAUDE report 12311845 ↗

Other Humidifier, Non-Direct Patient Interface (Home-Use) devices

All Humidifier, Non-Direct Patient Interface (Home-Use) devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.