Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Prescription Drugs
💊 Drugs • 12,141 recalls
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Atorvastatin Calcium 40mg Tablet, 30-count bottles, Rx only, Pk By Safecor Health Woburn, MA 01801, NDC 60505258009
Safecor Health
CGMP Deviations
Doxycycline100mg Tablets, 14-count bottles, Rx only, Packaged By Safecor Health LLC Woburn, MA 01801, NDC 0143314205
Safecor Health
CGMP Deviations
Acyclovir 400mg Tablet, 15-count bottles, Rx only, Packaged by Safecor Health, LLC. Woburn, MA 01801, NDC 0093894305
Safecor Health
CGMP Deviations
Metronidazole 500mg Tablet, 50-count bottles, Rx only, Packaged By Safecor Health LLC Woburn, MA 01801, NDC 5011133402
Safecor Health
CGMP Deviations
CGMP deviations- Lack of Quality Assurance
CGMP deviations- Lack of Quality Assurance
Failed Dissolution Specifications: out of specification results observed for low dissolution.
CGMP deviations- Lack of Quality Assurance
CGMP Deviations: these repackaged and redistributed products are being recalled due to a recall notice from the active pharmaceutical ingredient manufacturer for deviations from current Good Manufacturing Practices that were found during a recent FDA inspection.
CGMP deviations- Lack of Quality Assurance
CGMP deviations- Lack of Quality Assurance
Option 2, Levonorgestrel Tablet, 1.5 mg, Emergency Contraceptive, 1 Tablet per box, Distributed By Perrigo, Allegan, MI 49010. NDC 0113-2003-12
L. Perrigo Company
Defective Container: Carton is missing the tablet blister strip and tablet.
CGMP deviations- Lack of Quality Assurance
Failed Dissolution Specifications: out of specification results observed for low dissolution.
Presence of Foreign Substance: human hair melded into tablet.
CGMP deviations- Lack of Quality Assurance
Levonorgestrel, U.S.P. active pharmaceutical ingredient, packaged in 1 kg container, Rx only, Spectrum Chemical Mfg. Corp, Gardena, CA 90248, New Brunswick, NJ 08901, Product code L1229.
Spectrum Laboratory Products
CGMP Deviations: these repackaged and redistributed products are being recalled due to a recall notice from the active pharmaceutical ingredient manufacturer for deviations from current Good Manufacturing Practices that were found during a recent FDA inspection.
Failed Dissolution Specifications: out of specification results observed for low dissolution.