How many FDA warning letters has Uvlizer c/o RAIS INTERNATIONAL LLC received?

Argus HQ has not recorded an FDA warning letter for Uvlizer c/o RAIS INTERNATIONAL LLC in our current dataset.

What FDA recalls has Uvlizer c/o RAIS INTERNATIONAL LLC issued?

Argus HQ has recorded 2 FDA recalls tied to Uvlizer c/o RAIS INTERNATIONAL LLC.

Is Uvlizer c/o RAIS INTERNATIONAL LLC FDA compliant?

Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 2 recalls, and 0 approval records for Uvlizer c/o RAIS INTERNATIONAL LLC. Review the linked FDA source records directly before drawing a compliance conclusion.

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company

Uvlizer c/o RAIS INTERNATIONAL LLC

Name: FDA Enforcement Actions Against Uvlizer c/o RAIS INTERNATIONAL LLC
Creator: Argus HQ
License: https://argushq.ai/methodology

Jurisdiction: US

FDA Warning Letter timeline

V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.

fda_recall · device_recall2026-04-29
Uvlizer c/o RAIS INTERNATIONAL LLC — Class II recall: The product is a handheld ultraviolet-C germicidal wand and contains a combinati…
fda_recall · device_recall2026-04-29
Uvlizer c/o RAIS INTERNATIONAL LLC — Class II recall: The product is a handheld ultraviolet-C germicidal wand and contains two low-pre…

Frequently asked questions

How many FDA warning letters has Uvlizer c/o RAIS INTERNATIONAL LLC received?: Argus HQ has not recorded an FDA warning letter for Uvlizer c/o RAIS INTERNATIONAL LLC in our current dataset.
What FDA recalls has Uvlizer c/o RAIS INTERNATIONAL LLC issued?: Argus HQ has recorded 2 FDA recalls tied to Uvlizer c/o RAIS INTERNATIONAL LLC.
Is Uvlizer c/o RAIS INTERNATIONAL LLC FDA compliant?: Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 2 recalls, and 0 approval records for Uvlizer c/o RAIS INTERNATIONAL LLC. Review the linked FDA source records directly before drawing a compliance conclusion.

Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.