How many FDA warning letters has Oculus Technologies of Mexico, S.A. de C.V. received?

Argus HQ has not recorded an FDA warning letter for Oculus Technologies of Mexico, S.A. de C.V. in our current dataset.

What FDA recalls has Oculus Technologies of Mexico, S.A. de C.V. issued?

Argus HQ has recorded 1 FDA recall tied to Oculus Technologies of Mexico, S.A. de C.V..

Is Oculus Technologies of Mexico, S.A. de C.V. FDA compliant?

Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 1 recall, and 0 approval records for Oculus Technologies of Mexico, S.A. de C.V.. Review the linked FDA source records directly before drawing a compliance conclusion.

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company

Oculus Technologies of Mexico, S.A. de C.V.

Name: FDA Enforcement Actions Against Oculus Technologies of Mexico, S.A. de C.V.
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_recall2026-06-10
Oculus Technologies of Mexico, S.A. de C.V. — Class II recall: PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050

Frequently asked questions

How many FDA warning letters has Oculus Technologies of Mexico, S.A. de C.V. received?: Argus HQ has not recorded an FDA warning letter for Oculus Technologies of Mexico, S.A. de C.V. in our current dataset.
What FDA recalls has Oculus Technologies of Mexico, S.A. de C.V. issued?: Argus HQ has recorded 1 FDA recall tied to Oculus Technologies of Mexico, S.A. de C.V..
Is Oculus Technologies of Mexico, S.A. de C.V. FDA compliant?: Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 1 recall, and 0 approval records for Oculus Technologies of Mexico, S.A. de C.V.. 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.