Overview of recall records associated with Pharmaceutical Innovations, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 6.
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.
Potential for failed stability antimicrobial effectiveness testing.
Potential for failed stability antimicrobial effectiveness testing.
Potential for failed stability antimicrobial effectiveness testing.
This page summarizes recall records in which the official source identifies Pharmaceutical Innovations, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
