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The Health Sciences Authority (HSA) in Singapore oversees a post-market surveillance program to ensure the quality, safety, and efficacy of therapeutic products. A key aspect of this program is managing product defects. Manufacturers, importers, or suppliers are required to report any defects related to their products and notify HSA before initiating a recall. This video tutorial outlines the requirements and processes for defect reporting and product recalls. Defects can occur during manufacturing, storage, and handling, and it is crucial to report them, especially if they impact safety and efficacy. Timely reporting helps identify potential issues and protects public health.