Zinc Chloride (0.5 mg/mL), Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835, NDC 73198-0071-30
Olympia Compounding Pharmacy
Lack of assurance of sterility.
💊 Drugs • 11,927 recalls
Olympia Compounding Pharmacy
Lack of assurance of sterility.
Lack of assurance of sterility.
Preferred Pharmaceuticals
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Olympia Compounding Pharmacy
Lack of assurance of sterility.
Failed Dissolution Specifications: Nitrofurantoin Capsules recalled due to dissolution failure at 0-time of the repackaged lot. Drug release results were above specification at 0-time.
Subpotent drug: Low OOS for menthol content at the three month room temperature.
TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions
CGMP Deviations: Failure to properly investigate failed microbial testing.
CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions due to inclement weather.
Failed Dissolution Specifications: Sirolimus Oral Solution recalled due to lot RZ1598 exceeded the specification limit at the 14-month timepoint.
TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions due to inclement weather.
Lupin Pharmaceuticals
Failed Stability Specification
Does Not Meet USP or OTC Monograph: Product exceeds USP specification for alcohol content
Subpotent Drug
Mylan Institutional, Inc. (d.b.a. UDL Laboratories)
Failed Impurities/Degradation Specifications: OOS result was obtained for Any Other Individual Impurity at the 12M room temperature time point.
Failed Dissolution Specifications: low out of specification results for dissolution.
Presence Of Foreign Substance: Customer complaint for the presence of dark, gritty substance found within the bottle which was determined to be activated carbon from the desiccant canister inside the bottle.