Bicillin L-A
cGMP Deviations: Products were stored outside the drug label specifications.
Class II means the product may cause temporary or medically reversible harm, and serious harm is unlikely. It is by far the largest recall class - most potency, dissolution and labeling problems land here.
14,535 recalls, newest first.
cGMP Deviations: Products were stored outside the drug label specifications.
cGMP Deviations: Products were stored outside the drug label specifications.
cGMP Deviations: Products were stored outside the drug label specifications.
cGMP deviations: Temperature excursion due to shipping delay from manufacturer to distributor. Affected distributor has been notified.
cGMP deviations: Temperature excursion due to shipping delay from manufacturer to distributor. Affected distributor has been notified.
Failed Dissolution Specifications: Out of specification for dissolution.
Labeling: Incorrect or Missing Package Insert
Subpotent Drug: Out of specification for assay
CGMP Deviations: Inadequate induction sealing on bottles, capsules were observed with bubbles on band seal, capsules with holes and spheres sticking to capsules. Also coding details were missing on one bottle.
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility
CGMP Deviations
CGMP Deviations
Incorrect product concentration on the overwrap label: The overwrap label incorrectly identified the product strength as 4 mg / 250 mL; however, the primary bag label correctly identified the product strength as 8 mg / 250 mL.
Sub-potent drug: failure to maintain potency through the duration of the labeled expiration/beyond-use date.
CGMP Deviations: Potential Glass and Silicone particulates in product
CGMP Deviations: Potential Glass and Silicone particulates in product
CGMP Deviations: Potential Glass and Silicone particulates in product
CGMP Deviations: Potential Glass and Silicone particulates in product
CGMP Deviations: Potential Glass and Silicone particulates in product
CGMP Deviations
CGMP Deviations
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.