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Code of Federal Regulations (Last Updated: November 8, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter H - Medical Devices |
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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. |