Recall

An action taken to address a problem with a medical device that violates law or poses a health risk.

Recalls involve correcting, removing, or updating distributed devices due to defects, safety alerts, or performance failures. Regulators such as the FDA and MHRA mandate prompt reporting and risk-based categorization for recall actions.

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HaRi brings the FDA, MHRA, EUDAMED, Health Canada and TGA registers into one search: devices, manufacturers, product codes and safety events, all cross-referenced and free to explore.

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