Code of Federal Regulations (Last Updated: October 10, 2024) |
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 A - General Provisions |
§ 810.1 - Scope. |
§ 810.2 - Definitions. |
§ 810.3 - Computation of time. |
§ 810.4 - Service of orders. |
Subpart B - Mandatory Medical Device Recall Procedures |
§ 810.10 - Cease distribution and notification order. |
§ 810.11 - Regulatory hearing. |
§ 810.12 - Written request for review of cease distribution and notification order. |
§ 810.13 - Mandatory recall order. |
§ 810.14 - Cease distribution and notification or mandatory recall strategy. |
§ 810.15 - Communications concerning a cease distribution and notification or mandatory recall order. |
§ 810.16 - Cease distribution and notification or mandatory recall order status reports. |
§ 810.17 - Termination of a cease distribution and notification or mandatory recall order. |
§ 810.18 - Public notice. |