21 CFR Subpart C - Subpart C—Recalls (Including Product Corrections)—Guidance on Policy, Procedures, and Industry Responsibilities
- § 7.40 Recall policy.
- § 7.41 Health hazard evaluation and recall classification.
- § 7.42 Recall strategy.
- § 7.45 Food and Drug Administration-requested recall.
- § 7.46 Firm-initiated recall.
- § 7.49 Recall communications.
- § 7.50 Public notification of recall.
- § 7.53 Recall status reports.
- § 7.55 Termination of a recall.
- § 7.59 General industry guidance.
Source:
43 FR 26218, June 16, 1978, unless otherwise noted.