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Eugene Oregon, Inc.

Eugene Oregon, Inc. Recalls

All product recalls associated with Eugene Oregon, Inc..

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

May 2014

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–3 of 3 recalls

Mojo Risen Capsules (Eugene Oregon) – Undeclared Sildenafil (2014)

Undeclared Allergen

Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.

Class IHigh

FDAMay 5, 2014FL, IL, IN +8 more• Eugene Oregon, Inc.

Black Ant Capsules (Eugene Oregon) – Undeclared Sildenafil (2014)

Undeclared Allergen

Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.

Class IHigh

FDAMay 5, 2014FL, IL, IN +8 more• Eugene Oregon, Inc.

African Black Ant Capsules (Eugene Oregon) – Undeclared Sildenafil (2014)

Undeclared Allergen

Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.

Class IHigh

FDAMay 5, 2014FL, IL, IN +8 more• Eugene Oregon, Inc.