Alfuzosin Hydrochloride Extended-release Tablets
Presence of Foreign Substance: consumer complaint for foreign matter embedded in the tablet identified as a broken piece of wire rope from the manufacturing equipment.
11,818 recalls · Class II, newest first
Presence of Foreign Substance: consumer complaint for foreign matter embedded in the tablet identified as a broken piece of wire rope from the manufacturing equipment.
Failed Dissolution Specifications; 18 month stability time point
Failed Dissolution Specifications; 18 month stability time point
Failed Dissolution Specifications; 18 month stability time point
Failed Dissolution Specifications; 18 month stability time point
Microbial Contamination of Non-Sterile Product; small number of tubes may include the presence of mold on the cap
Failed Tablet/Capsule Specifications: Some bottles contain punctured, and/or clumped/melted capsules.
Failed Tablet/Capsule Specifications: An unusually thick tablet was reported through a complaint.
Failed dissolution specification: recalled due to an out of specification dissolution result of 40% (Specification: NLT 80%)
Subpotency: due to a low, out of specification test result for assay during stability testing.
Failed tablet/capsule specification: missing break line on the 5mg tablet.
Failed Tablet/Capsule Specifications: customer complaints of broken or crushed capsules, resulting in loose powder in the bottle.
Failed Tablet/Capsule Specifications: customer complaints of broken or crushed capsules, resulting in loose powder in the bottle.
Failed Tablet/Capsule Specifications: customer complaints of broken or crushed capsules, resulting in loose powder in the bottle.
Failed Tablet/Capsule Specifications: customer complaints of broken or crushed capsules, resulting in loose powder in the bottle.
Failed Impurities/Degradation Specifications
CGMP Deviations
CGMP Deviations
Lack of Sterility Assurance
Lack of Assurance of Sterility: Potential cracks in glass vials
CGMP Deviations
CGMP Deviations
Failed Dissolution Specifications
Discoloration: there were customer reports of yellow discolored solution. The yellow coloration is the result of oxidation of the amino acid tryptophan due to a damaged overpouch.
Lack of Assurance of Sterility: confirmed customer complaints of leaking bags.