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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, and suppliers are obligated to report any product defects and notify HSA before initiating product recalls. Defects can occur during manufacturing, storage, or handling, and it is crucial to report these to safeguard public health. This video provides essential information on the requirements and processes for defect reporting and product recalls, aiming to protect users and ensure proper measures are taken in response to safety concerns.