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All product recalls associated with Basic Reset Inc..
Total Recalls
1000
Past Year
566
Class I (Serious)
25
Most Recent
Jan 2026
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.
Marketed without an Approved NDA/ANDA
Marketed without an Approved NDA/ANDA
Marketed without an Approved NDA/ANDA
Marketed without an Approved NDA/ANDA
Marketed without an Approved NDA/ANDA
FDA determined that marketing claims surrounding product rendered product a medical device which was adulterated and misbranded.
Marketed without an Approved NDA/ANDA
Marketed without an Approved NDA/ANDA
Marketed without an Approved NDA/ANDA
Marketed without an Approved NDA/ANDA
Marketed without an Approved NDA/ANDA
The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.
The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.
The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.
The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.