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Code of Federal Regulations › Title 21 › Part 810

Part 810 — Medical Device Recall Authority

Current through Sep 8, 2026

Authority: 21 U.S.C. 321, 331, 332, 333, 334, 351, 352, 355, 360h, 360i, 371, 374, 375.

Source: 61 FR 59018, Nov. 20, 1996, unless otherwise noted.

Sections

  • § 810.1 Scope.
  • § 810.2 Definitions.
  • § 810.3 Computation of time.
  • § 810.4 Service of orders.
  • § 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.
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