Yager's Liniment
CGMP Deviations: Products not manufactured under current good manufacturing practices.
18,003 recalls, newest first
CGMP Deviations: Products not manufactured under current good manufacturing practices.
CGMP Deviations: Products not manufactured under current good manufacturing practices.
Labeling: Incorrect or Missing Lot and/or Exp Date: vials were labeled with the incorrect lot number and expiration date
Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil an ingredient found in a FDA approved product for the treatment of male sexual enhancement, making this an unapproved drug.
Failed dissolution specifications - results obtained were below spec average.
CGMP Deviations
CGMP Deviations
CGMP Deviations
CGMP Deviations
CGMP Deviations
Labeling: Not Elsewhere Classified - the description, warnings, storage information and instructions for use are either missing or partially printed.
Failed Impurities/Degradation Specifications
cGMP deviations: Batch was released prior to approval.
cGMP deviations: Batch was released prior to approval.
CGMP deviation: product released prior to supplier approval.
cGMP deviations: due to shipment of rejected units.
Failed Impurities/Degradation Specifications: Out-of-specification results observed for the organic impurities test at 6 months, RT Stability.
Out of Specification result observed in content uniformity testing
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Lack of assurance of sterility: Lack of validation data for sanitization cycles