L-Cysteine Hydrochloride Injection
Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing firm raised concerns that the product sterility may be compromised.
1,103 recalls, newest first
Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing firm raised concerns that the product sterility may be compromised.
Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing firm raised concerns that the product sterility may be compromised.
Labeling: Incorrect or Missing Lot and/or Exp Date - Product is missing or has illegible lot and expiry codes, as well as defective or cracked caps.
Superpotent
Labeling: Label Error on Declared Strength: Some bottles miss a color coded panel where the strength of the product is typically displayed.
Failed Impurities/Degradation Specifications: OOS results for known compound.
Failed Dissolution Specifications; 6 month time point
Lack of Assurance of Sterility: product produced on a day there was an excursion in environmental monitoring data.
Lack of Assurance of Sterility: product produced on a day there was an excursion in environmental monitoring data.
Presence of Foreign Tablets/Capsules; report of Amlodipine Tablets found in 1000 count bottles of Metformin Hydrochloride Tablets USP
Failed Content Uniformity: Product was out of specification for spray content uniformity obtained during stability testing.
Failed Content Uniformity: Product was out of specification for spray content uniformity obtained during stability testing.
Lack of Assurance of Sterility: Complaints of broken tips on the ampules.
Marketed without an approved NDA/ANDA: presence of undeclared sibutramine, desmethylsibutramine (an active metabolite of sibutramine) and phenolphthalein.
CGMP Deviations: manufactured under practices which may result in assay or content uniformity failures.
CGMP Deviations: manufactured under practices which may result in assay or content uniformity failures.
CGMP Deviations: manufactured under practices which may result in assay or content uniformity failures.
CGMP Deviations: manufactured under practices which may result in assay or content uniformity failures.
Failed Stability Specifications: Low Out of Specification results for alcohol content.
Failed Dissolution Specifications: The firm was notified that there was a dissolution out of specification result on the 6 month stability samples.
CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures
CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures
CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures
CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures
CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures