NorthStar Arthritis Relief Cream. Net Wt. 2 oz tube
Microbial Contamination of Non-Sterile Products: Arthritis Relief Cream failed microbiological specifications.
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Microbial Contamination of Non-Sterile Products: Arthritis Relief Cream failed microbiological specifications.
Lack of Assurance of Sterility; potential that a low level of endotoxins may be present in the diluent vials.
Subpotent; 22 month stability timepoint
Subpotent; 12 month stability timepoint
Presence of Particulate Matter; fibers identified as cellulose and polyvinyl
Presence of Particulate Matter; fibers identified as cellulose and polyvinyl
Lack of Assurance of Sterility: Complains of a loose crimp applied to the fliptop vial; and a missing stopper and flip cap were received and therefore sterility cannot be assured.
Product Lacks Stability: Out-of-specification (OOS) results were observed for assay and description in retain samples.
Failed Dissolution Test Requirements
Defective Container: Pump head detaching from the canister unit upon removal of the overcap.
Subpotent; 15 month stability (by mfr)
Presence of Particulate Matter: Visible particulate and particulate embedded in vials were observed during retain inspection.
Presence of Particulate Matter: Certain batches of Atorvastatin tablets 10 mg, 20 mg and 40 mg may contain small glass particulates.
Presence of Particulate Matter: Certain batches of Atorvastatin tablets 10 mg, 20 mg and 40 mg may contain small glass particulates.
Presence of Particulate Matter: Certain batches of Atorvastatin tablets 10 mg, 20 mg and 40 mg may contain small glass particulates.
Crystallization: Product is being recalled due to visible particulates identified during a retain sample inspection. Findings have identified the particles as Carboplatin crystals.
Crystallization: Product is being recalled due to visible particulates identified during a retain sample inspection. Findings have identified the particles as Carboplatin crystals.
Labeling Illegible: Portions of the product labeling in the area of the dosing directions, the warnings & other information sections is obscured.
Lack of Assurance of Sterility: Product did not meet the criteria for container closure integrity testing during routine 24 month stability testing.
Adulterated Presence of Foreign Tablets: A customer complaint was received that a bottle of Tramadol HCl Tablets USP 50 mg contained some tablets of Metoprolol Tartrate Tablets USP, 50 mg.
Defective container; damaged bottles could allow moisture to get into the bottle and thus may impair the quality of the product
CGMP Deviations: A drum of Abilify 30 mg Tablets rejected during the compression stage was not segregated from the other portion of the lot and was inadvertently shipped, packaged and distributed.
GMP deficiencies
Lack of assurance of sterility
Subpotent; 15 month stability