Skip to content

VicksRecalls & reported problems across all models

Kaz USA, Inc. · 12 models in the FDA device registry

Data updated Oct 16, 2026 from official FDA records · Editorial policy

1 open recall names at least one Vicks model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.

Adverse event reports
42
Deaths reported
1
Injuries reported
37
Recalls
1

We found 12 models of Vicks by Kaz USA, Inc. in the FDA's device registry (GUDID). Together they are named in 42 adverse event reports in the FDA's MAUDE database, received between Mar 22, 2019 and Jun 19, 2026 — classified as 1 death, 37 injuries, 4 malfunctions.

The most frequently reported specific device problem is “Use of Device Problem” (34 reports).

1 FDA recall record name at least one of these models by its device identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Reports received per month, all models

Nov 2023: 1 reportsDec 2023: 0 reportsJan 2024: 2 reportsFeb 2024: 0 reportsMar 2024: 1 reportsApr 2024: 0 reportsMay 2024: 1 reportsJun 2024: 0 reportsJul 2024: 1 reportsAug 2024: 1 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 1 reportsFeb 2025: 0 reportsMar 2025: 1 reportsApr 2025: 1 reportsMay 2025: 1 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 2 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 1 reportsFeb 2026: 1 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 1 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Vicks recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

  1. Mar 16, 2021Open, Classified

    Due to shipping delays the devices were exposed to temperature excursions of 31.9F, intermittently over a 2 hour and 15 minute period of time which may cause inaccurate results.

    Z-1935-2021 · Root cause: Environmental control · Recall details · FDA record ↗

Most reported Vicks problems

Device problems

  • Use of Device Problem34
  • Patient Device Interaction Problem27
  • Device Handling Problem17
  • Human-Device Interface Problem12
  • Unexpected Therapeutic Results8
  • False Negative Result4
  • Device Tipped Over3
  • Insufficient Device Problem Information3

Patient problems

  • Partial thickness (Second Degree) Burn23
  • Full thickness (Third Degree) Burn7
  • Burn(s)6
  • Fever4
  • Blister1
  • Caustic/Chemical Burns1
  • Cough1
  • Discomfort1

Vicks models

12 models, most reported first. Each model has its own page with its reports, recalls and device details.

Recent Vicks adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

Other Kaz USA, Inc. products

All Kaz USA, Inc. devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page