Walgreens 2100-WGNRecalls & reported problems
Walgreen CO. · Vaporizer 1.0 Gallon · Class 1
All models of Walgreens (38)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00049022459779), received between Jan 28, 2022 and Oct 12, 2022 — classified as 2 injuries.
The most frequently reported specific device problem is “Use of Device Problem” (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.
Most reported problems
Device problems
- Use of Device Problem2
- Patient Device Interaction Problem1
- Unexpected Therapeutic Results1
Patient problems
- Full thickness (Third Degree) Burn1
- Partial thickness (Second Degree) Burn1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryOct 12, 2022Use of Device Problem; Patient Device Interaction Problem; Use of Device Problem; Patient Device Interaction Problem
A CONSUMER CALLED AND STATED THAT THEIR CHILD ACCIDENTALLY GOT TANGLED WITH THE VAPORIZER'S CORD DURING OPERATION, WHICH CAUSED THE UNIT TO SPILL HOT WATER ONTO THE CHILD. THE CHILD RECEIVED MEDICAL TREATMENT AT AN EMERGENCY ROOM FOR SECOND DEGREE BURNS, AND SHE ALSO REQUIRED FOLLOW UP CARE FOR THESE INJURIES. THE INSTRUCTIONS FOR PROPER USE HAVE VERY CLEAR WARNINGS THAT STATE,"WARNING: KEEP OUT OF REACH OF CHILDREN", AS WELL AS "THE VAPORIZER SHOULD ALWAYS BE PLACED ON A FIRM, FLAT, WATERPROOF, SURFACE AT LEAST FOUR FEET AWAY FROM BEDSIDE, SIX INCHES FROM THE WALL AND OUT OF THE REACH OF CHILDREN AND PETS. BE SURE APPLIANCE IS IN A STABLE POSITION AND THE POWER CORD IS AWAY FROM HEATED SURFACES AND OUT OF THE WAY TO PREVENT THE VAPORIZER FROM BEING OVERTURNED."
Patient problems: Partial thickness (Second Degree) Burn
MAUDE report 15589472 ↗InjuryJan 28, 2022Unexpected Therapeutic Results; Use of Device Problem; Unexpected Therapeutic Results; Use of Device Problem
A CONSUMER REPORTED THAT SHE RECEIVED THIRD DEGREE BURNS ON HER ARM FROM THE HOT STEAM THAT WAS BEING PRODUCED BY THE VAPORIZER DURING USE. SHE STATED THAT HER INJURIES OCCURRED WHEN SHE QUICKLY REACHED OVER THE STEAM OUTPUT DURING USE. MEDICAL INTERVENTION WAS SOUGHT FOR HER INJURIES SIX DAYS AFTER THE INCIDENT OCCURRED. THE INSTRUCTIONS FOR PROPER USE HAVE CLEAR WARNINGS WHICH STATE "DO NOT TOUCH THE STEAM VAPOR. STEAM CAN CAUSE BURNS.", AS WELL AS A WARNING ON THE DEVICE ITSELF WHICH STATES, "WARNING KEEP OUT OF REACH OF CHILDREN HOT STEAM CAN CAUSE SERIOUS BURN INJURY." KAZ USA, INC. HAS REQUESTED THAT THE PRODUCT BE RETURNED TO OUR COMPANY FOR TESTING.
Patient problems: Full thickness (Third Degree) Burn
MAUDE report 13388766 ↗
Other Humidifier, Non-Direct Patient Interface (Home-Use) devices
- Vicks V150GLKaz USA, Inc. · Humidifier, Non-Direct Patient Interface (Home-Use)1 recall1 report
- Vicks VIH200Kaz USA, Inc. · Humidifier, Non-Direct Patient Interface (Home-Use)16 reports
- VICKS V1200-6-VV1Kaz USA, Inc. · Humidifier, Non-Direct Patient Interface (Home-Use)13 reports
- Vicks VWM845Kaz USA, Inc. · Humidifier, Non-Direct Patient Interface (Home-Use)1 death2 reports
- Vicks VIH200V4Kaz USA, Inc. · Humidifier, Non-Direct Patient Interface (Home-Use)2 reports
- Mabis 40-741-000D-M-S Holdings, Inc. · Humidifier, Non-Direct Patient Interface (Home-Use)2 reports
- Vicks V745AKaz USA, Inc. · Humidifier, Non-Direct Patient Interface (Home-Use)1 report
- CVS GVP110Woonsocket Prescription Center, Incorporated · Humidifier, Non-Direct Patient Interface (Home-Use)1 report
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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