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Business · 22/02/2013Updated: 10/17/2026 · 1 min read

FDA Releases Draft Guidance on Distinguishing Medical Device Recalls from Product Enhancements

Summary

The Food and Drug Administration (FDA) has published a draft guidance to help industry staff differentiate between medical device recalls and product enhancements, outlining reporting requirements for both.

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

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