Sterile Curcumin
Reason Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA: Product contains unapproved Cannabidiol and Curcumin
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Reason Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA: Product contains unapproved Cannabidiol and Curcumin
Reason Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA: Product contains unapproved Cannabidiol and Curcumin
Reason Failed Dissolution Specifications
Reason Presence of Particulate Matter: confirmed customer complaint for the presence of particulate matter identified as iron oxide.
Reason Short Fill
Reason Discoloration: Out-of-specification results for appearance obtained during routine stability testing at the end of shelf-life for the parameters Appearance and Color of Solution.
Reason Failed dissolution specifications: Low stage 3 results obtained for dissolution during routine stability testing.
Reason Discoloration: product contains brown pellets
Reason Presence of Particulate Matter: Fresenius Kabi recalling vials of Ketorolac
Reason Defective Container: Sub-optimal crimping in vial of Pediatric Infuvite Multiple Vitamins
Reason Presence of Particulate Matter - found in reserve sample vials at the firm.
Reason Presence of Particulate Matter - found in reserve sample vials at the firm.
Reason Labeling: Not elsewhere classified: Observed separation in the secondary packaging in the blister and the backer card
Reason Labeling: Not elsewhere classified: Observed separation in the secondary packaging in the blister and the backer card
Reason Labeling: Not elsewhere classified: Observed separation in the secondary packaging in the blister and the backer card
Reason Product Mix-Up: a complaint received indicating mix-up of 10 mg Lisinopril tablets inside of 2 sealed bottles of 20 mg/1000 count bottles.
Reason Failed Stability Specifications: Out-of-Specification (OOS) results for High Molecular Weight Polymers.
Reason Chemical Contamination; product contains elevated levels of lead
Reason CGMP Deviations: potential N-Nitrosodimethylamine (NDMA) amounts above levels established by the FDA.
Reason Subpotent Drug: low out of specification (OOS) test result observed in long term stability study.
Reason cGMP Deviations
Reason Cross Contamination with Other Products; Finasteride Plus 1.25mg capsules were found to contain minoxidil.
Reason cGMP deviations: Presence of foreign material (Teflon)introduced at the production level.
Reason Lack of Processing Control
Reason Lack of Processing Control