Actavis Elizabeth LLC

Complete recall history across all FDA and CPSC categories — 14 total recalls

Actavis Elizabeth LLC appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Drug Recalls (14)

FDA drug safety enforcement actions by Actavis Elizabeth LLC

Date Product Reason Class
Oct 6, 2016 NIFEdipine Capsules USP, 10 mg, Rx only, 100 count bottle, Manufactured and d... Presence of Foreign Tablets/Capsules Class III
Feb 16, 2016 Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfat... Failed Impurities/Degradation Specifications: Out of specification for impuri... Class II
Feb 16, 2016 Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfat... Failed Impurities/Degradation Specifications: Out of specification for impuri... Class II
Feb 16, 2016 Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfat... Failed Impurities/Degradation Specifications: Out of specification for impuri... Class II
Feb 16, 2016 Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfat... Failed Impurities/Degradation Specifications: Out of specification for impuri... Class II
Feb 10, 2015 Dextroamphetamine Sulfate Extended-Release Capsules, 15 mg, 90-count bottles,... Failed Dissolution Specifications Class II
Dec 15, 2014 Gabapentin Capsules, USP, 100 mg, Rx Only, a) 100 capsules per bottle, NDC 45... Failed Capsule/Tablet Specifications: Actavis has received several complaint ... Class II
Dec 15, 2014 Gabapentin Capsules, USP, 400 mg, Rx Only, a) 100 capsules per bottle, NDC 14... Failed Capsule/Tablet Specifications: Actavis has received several complaint ... Class II
Dec 15, 2014 Gabapentin Capsules, USP, 300 mg, Rx Only, 100 capsules per bottle, Manufactu... Failed Capsule/Tablet Specifications: Actavis has received several complaint ... Class II
Feb 10, 2014 Alprazolam 1 mg Tablets, USP, 500 count Bottle, Rx Only , C IV, Manufactured ... Failed Tablet/Capsule Specifications: Complaints were received for significan... Class II
Feb 4, 2014 Alprazolam Extended-Release Tablets, USP, 3 mg, 60-count tablets per bottle, ... Failed Dissolution Specifications: Product did not meet specification require... Class II
Nov 6, 2013 Clonazepam Tablets, USP 2 mg 100 tablets Manufactured by: Actavis Elizabeth L... Subpotent Drug: During routine stability testing one tablet was found with ta... Class II
Oct 9, 2013 Alprazolam Orally Disintegrating Tablets, USP 2 mg, 100 count bottles, Rx Onl... Failed Tablet/Capsule Specifications; partial tablet erosion resulting in tab... Class II
Feb 13, 2013 Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphet... Failed Dissolution Specification: This product recall is due to the product l... Class III

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

Explore More Recalls

Search recalls by category, state, reason, or firm across all our databases.