GroundRules
21 CFR 810.18: Public notice.
Where this section sits in the code
- Title 21—Food and Drugs
- CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
- SUBCHAPTER H—MEDICAL DEVICES
- PART 810—MEDICAL DEVICE RECALL AUTHORITY
- Subpart B—Mandatory Medical Device Recall Procedures
The agency will make available to the public in the weekly FDA Enforcement Report a descriptive listing of each new mandatory recall issued under § 810.13. The agency will delay public notification of orders when the agency determines that such notification may cause unnecessary and harmful anxiety in individuals and that initial consultation between individuals and their health professionals is essential.
Collected 2026-08-27T02:24:47Z. Source file · JSON