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FDA Medical Device Recalls with AI Analysis

The FDA publishes medical device recalls via an open API. This is public data, but it is raw records without prioritization or explanation of consequences. We collect fresh recalls and provide an AI analysis for each: what the device is, who the manufacturer is, the reason for the recall, and what it means for distributors, clinics and importers. The signal is critical if you supply medical devices, run a clinic, or import products: the cost of a mistake is a recalled batch and direct losses.

Source
openFDA (device/recall)
Refresh: every 24 h · Access windows: 24 h / 7 d / 30 d

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