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Business · 15/10/2014Updated: 10/17/2026 · 1 min read

FDA Releases Guidance on Distinguishing Medical Device Recalls from Enhancements

Summary

The Food and Drug Administration (FDA) has issued a guidance document to help industry professionals and FDA staff identify medical device recalls and product enhancements, outlining reporting requirements for the latter.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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