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All product recalls associated with Pharmaceutical Innovations, Inc..
Total Recalls
3
Past Year
0
Class I (Serious)
0
Most Recent
Aug 2020
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.
The firm registered the product as a Class I device, but has since been informed by FDA that the device is not Class I and requires a 510(k) submission.
Potential for failed stability antimicrobial effectiveness testing.
Potential for failed stability antimicrobial effectiveness testing.