GlipiZIDE Extended-Release Tablets
Reason Failed Dissolution Specifications: results were above specification.
17,898 recalls, newest first
Reason Failed Dissolution Specifications: results were above specification.
Reason CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with microbial organisms.
Reason CGMP deviations: Gaps in the quality system in the Quality Control microbiology laboratory.
Reason Failed Impurities/Degradation Specifications; out of specification for Related Compound
Reason Labeling: Label Lacks Warning or Rx Legend: Finished product did not include the statement on the flip cap vial, "WARNING: PARALYZING AGENT"
Reason Presence of Foreign Substance: Product complaints received for the presence of metal wire in one tablet.
Reason Labeling: Label Mix-Up.The recall has been initiated after receiving one complaint about incorrect labeling.The primary label on the front and back label on some of the bottles have 70% Isopropyl Alcohol affixed to the containers. However, the product inside the bottle is Hydrogen Peroxide, Topical Solution USP with active ingredient Hydrogen Peroxide (stabilized) 3%, 32 FL Ounces
Reason Microbial contamination of non-sterile products: Firm's testing found lots to exceed specification for aerobic bacteria, yeast, and mold counts.
Reason Lack of Assurance of Sterility
Reason CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with microbial organisms.
Reason CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with microbial organisms.
Reason CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with microbial organisms.
Reason Presence of Particulate Matter: Particulate matter identified as fibers, hair, and proteinaceous material along with other particles, found in retain smples.
Reason Failed Impurities/Degradation Specifications
Reason Subpotent Drug
Reason Subpotent Drug
Reason Labeling: Incorrect Instructions
Reason Subpotency: one product for active ingredient assay and another one for preservative assay
Reason Subpotency: one product for active ingredient assay and another one for preservative assay
Reason Microbial Contamination of Non-Sterile Product: Out-of-specification results obtained for total aerobic microbial count (TAMC).
Reason Lack of Assurance of Sterility
Reason CGMP Deviations
Reason CGMP Deviations
Reason CGMP Deviations
Reason CGMP Deviations