DrugMar 5, 2014
Actavis Gelnique (oxybutynin chloride) Gel 10%, 100 mg in 1 g sachet, for topical use only recall — FDA D-1088-2014
Subpotent Drug: Drug potency was compromised during shipment.
Class IIIFDA: TerminatedActavis
Recall history in this database
Classification mix: Class III: 1, Class II: 1.
DrugOct 3, 2012
Actavis Fentanyl Transdermal System, 100 mcg/h, each transdermal system contains: 10 mg recall — FDA D-1693-2012
Subpotent; some patches may not contain fentanyl gel
Class IIFDA: TerminatedActavis
Understanding this recall history
This page summarizes recall records in which the official source identifies Actavis 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.