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Actavis Elizabeth Recalls
14 recalls on record · March 13, 2013 to November 30, 2016 · Drugs
Recalls by year
13
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16
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
November 30, 2016DrugsFDA
Actavis Elizabeth LLC recalls NIFEdipine Capsules USP, 10 mg, Rx only, 100 count bottle, Manufactured and distributed by: Actavis Elizabeth LLC, 200 E
Hazard: Presence of Foreign Tablets/Capsules
April 13, 2016DrugsFDA
Actavis Elizabeth LLC recalls Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 5 mg, 1
Hazard: Failed Impurities/Degradation Specifications: Out of specification for impurities.
April 13, 2016DrugsFDA
Actavis Elizabeth LLC recalls Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 30 mg,
Hazard: Failed Impurities/Degradation Specifications: Out of specification for impurities.
April 13, 2016DrugsFDA
Actavis Elizabeth LLC recalls Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 20 mg,
Hazard: Failed Impurities/Degradation Specifications: Out of specification for impurities.
April 13, 2016DrugsFDA
Actavis Elizabeth LLC recalls Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 10 mg,
Hazard: Failed Impurities/Degradation Specifications: Out of specification for impurities.
March 11, 2015DrugsFDA
Actavis Elizabeth LLC recalls Dextroamphetamine Sulfate Extended-Release Capsules, 15 mg, 90-count bottles, Rx Only, Manufactured by: Actavis Elizabe
Hazard: Failed Dissolution Specifications
January 14, 2015DrugsFDA
Actavis Elizabeth LLC recalls Gabapentin Capsules, USP, 100 mg, Rx Only, a) 100 capsules per bottle, NDC 45963-555-11, b) 500 Capsules per bottle, NDC
Hazard: Failed Capsule/Tablet Specifications: Actavis has received several complaint for clumping and breaking of capsules with some bottles showing popped out bottle bottom (round bottom) and creased labels from one distribution center.
January 14, 2015DrugsFDA
Actavis Elizabeth LLC recalls Gabapentin Capsules, USP, 300 mg, Rx Only, 100 capsules per bottle, Manufactured by: Actavis Pharma Manufacturing Pvt. L
Hazard: Failed Capsule/Tablet Specifications: Actavis has received several complaint for clumping and breaking of capsules with some bottles showing popped out bottle bottom (round bottom) and creased labels from one distribution center.
January 14, 2015DrugsFDA
Actavis Elizabeth LLC recalls Gabapentin Capsules, USP, 400 mg, Rx Only, a) 100 capsules per bottle, NDC 14550-513-02, b) 500 Capsules per bottle, NDC
Hazard: Failed Capsule/Tablet Specifications: Actavis has received several complaint for clumping and breaking of capsules with some bottles showing popped out bottle bottom (round bottom) and creased labels from one distribution center.
March 19, 2014DrugsFDA
Actavis Elizabeth LLC recalls Alprazolam 1 mg Tablets, USP, 500 count Bottle, Rx Only , C IV, Manufactured by: Actavis Elizabeth LLC 200 Elmora Avenue
Hazard: Failed Tablet/Capsule Specifications: Complaints were received for significant tablet erosion for Alprazolam 1 mg.
March 12, 2014DrugsFDA
Actavis Elizabeth LLC recalls Alprazolam Extended-Release Tablets, USP, 3 mg, 60-count tablets per bottle, Rx only, Manufactured by: Actavis Elizabet
Hazard: Failed Dissolution Specifications: Product did not meet specification requirements for dissolution.
March 5, 2014DrugsFDA
Actavis Elizabeth LLC recalls Clonazepam Tablets, USP 2 mg 100 tablets Manufactured by: Actavis Elizabeth LLC 200 Elmora Avenue, Elizabeth, NJ 0737 US
Hazard: Subpotent Drug: During routine stability testing one tablet was found with tablet weight below specification.
December 4, 2013DrugsFDA
Actavis Elizabeth LLC recalls Alprazolam Orally Disintegrating Tablets, USP 2 mg, 100 count bottles, Rx Only, MFG. BY ACTAVIS ELIZABETH LLC., Elizabet
Hazard: Failed Tablet/Capsule Specifications; partial tablet erosion resulting in tablet weights below specification in some tablets
March 13, 2013DrugsFDA
Actavis Elizabeth LLC recalls Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate Extended
Hazard: Failed Dissolution Specification: This product recall is due to the product lot # 50077231 exceeding dissolution specifications. All other test specifications were met.