Actavis Albuterol Sulfate Inhalation Solution, USP, 0.021% (0.63 mg / 3 mL), 3mL Vials recall — FDA D-0439-2017
Failed Impurities/Degradation Specifications: Product is out of specification for a known degradant.
Overview of recall records associated with Actavis Inc., including dates, categories and classifications where available.
Classification mix: Class III: 4.
Failed Impurities/Degradation Specifications: Product is out of specification for a known degradant.
Failed Impurities/Degradation Specifications: Out of specification (OOS) results for related compound G were obtained at 12-month (at expiry) stability time-point for room temperature…
Failed Impurities/Degradation Specifications: Out of specification (OOS) results for related compound G were obtained at 12-month (at expiry) stability time-point for room temperature…
Labeling: Incorrect or Missing Package Insert; Product is being recalled because the birth control packs were distributed with out-dated package inserts.
This page summarizes recall records in which the official source identifies Actavis 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.