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All product recalls associated with Ben Venue Laboratories Inc.
Total Recalls
1000
Past Year
558
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.
Lack of Assurance of Sterility: Crimp defects during visual inspection could affect container closure integrity.
Mindray DS USA Inc. initiated a voluntary field corrective action for V-Series Patient Monitor because there is an issue with the V-Series Drug Calculator function.
Lack of Assurance of Sterility; complaints of mold in the overpouch