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All product recalls associated with Allergan PLC.
Total Recalls
44
Past Year
0
Class I (Serious)
1
Most Recent
Mar 2024
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 action was initiated following notification by the U.S. FDA of their recently updated, global safety information concerning the higher incidence of anaplastic large cell lymphoma (BIA-ALCL) in patients who have textured breast implants.
The action was initiated following notification by the U.S. FDA of their recently updated, global safety information concerning the higher incidence of anaplastic large cell lymphoma (BIA-ALCL) in patients who have textured breast implants.
The action was initiated following notification by the U.S. FDA of their recently updated, global safety information concerning the higher incidence of anaplastic large cell lymphoma (BIA-ALCL) in patients who have textured breast implants.
cGMP Deviations
GMP Deviations: A silicone particulate was noted in Ozurdex.
Failed Stability Specification: out of specification for iron content.
Contraceptive Tablets Out of Sequence.
Labeling: Not Elsewhere Classified: does not have the required "CII" controlled drug classification indication on the primary label.
Failed Stability Specifications: Product stability testing results did not meet specifications for iron content.
Subpotent Drug: One lot of Viokace is being recalled since product stability testing results did not meet the specifications for enzyme profile.
Failed Impurities/Degradation Specifications.
Failed Impurities/Degradation Specifications.
Failed Impurities/Degradation Specifications: stability testing results did not meet the specification for impurities.
Failed Impurities/Degradation Specifications
Failed Content Uniformity Specifications
Failed Content Uniformity Specifications
Failed Content Uniformity Specifications.
Failed Content Uniformity Specifications.
Presence of Particulate Matter: Due to customer complaints of small black particles, identified as part of the ointment tube cap, generated by the action of unscrewing the cap from the aluminum tube and potentially introducing the particle into the product.
Presence of Particulate Matter: Due to customer complaints of small black particles, identified as part of the ointment tube cap, generated by the action of unscrewing the cap from the aluminum tube and potentially introducing the particle into the product.