21 CFR Part 810 — Medical Device Recall Authority
Subpart A — General Provisions
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.