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