Thyroid Tablets
Superpotent Drug
Class I is the FDA's most serious recall category: a reasonable probability that using the product will cause serious health consequences or death. It is a small share of all recalls, but the one to check first if a medication you take appears here.
1,750 recalls, newest first.
Superpotent Drug
Presence of Particulate Matter: particulate matter identified as iron oxide, inorganic material, cellulose cotton fiber or polystyrene
Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution.
Presence of particulate matter: Particulates identified as fiberglass
Presence of Particulate matter.
Presence of Particulate Matter and Lack of Assurance of Sterility. Particulate matter identified as nylon, cellulosic, acrylic, polyethylene and glass and broken and leaking vials.
Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles.
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
Labeling: Label Mixup: MicroVault labeled as Morphine 2 mg/1 mL, contains a Prefilled Syringe of Dilaudid 0.5 mg/0.5 mL.
Presence of Particulate Matter: comprising polyethylene and other plastic materials, stainless steel and glass.
Presence of Particulate Matter: Product contaminated with particulate matter identified as glass and/or paraformaldehyde
Presence of Particulate Matter
Presence of Particulate Matter; identified as stainless steel
Presence of Particulate Matter; identified as stainless steel
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
Cross Contamination with Other Products: Customer complaints for appearance of discolored tablets and red dots observed on Cetirizine Hydrochloride Tablets USP 5 mg. Determined to be Ranitidine.
Chemical Contamination: contamination with a diluted propylene glycol-based coolant from a machine leakage during the packaging process.
Microbial Contamination of Non-Sterile Products
Non-Sterility: Due to presence of Aspergillus penicillioides. And Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.
Non-Sterility: Due to presence of Aspergillus penicillioides.
Presence of Particulate matter: Particulate matter identified as glass.
Presence of Particulate Matter.
Microbial Contamination of Non-Sterile Products: confirmed presence of Staphylococcus Aureus.
Microbial contamination of Non-Sterile Product: samples identified the presence of Lysinibacillus fusiformis and other Bacillus spp
Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.