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All product recalls associated with Mayne Pharma Inc.
Total Recalls
6
Past Year
0
Class I (Serious)
0
Most Recent
Jun 2022
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.
Defective Delivery System: Out of specification for release liner removal force results at the 3-month CRT stability timepoint.
CGMP Deviation: Difficulty dispensing/does not dispense or dispensing liquid instead of foam.
Product Mix-Up: A foreign tablet was found in bottle.