Title 21

PART 7 SUBPART C

Subpart C - Recalls (Including Product Corrections) - Guidance on Policy, Procedures, and Industry Responsibilities Source:43 FR 26218, June 16, 1978, unless otherwise noted.

• 21 U.S.C. 321-393; 42 U.S.C. 241, 262, 263b-263n, 264.
• Source: 42 FR 15567, Mar. 22, 1977, unless otherwise noted.

21:1.0.1.1.7.3.63.1	SECTION 7.40	7.40 Recall policy.
21:1.0.1.1.7.3.63.2	SECTION 7.41	7.41 Health hazard evaluation and recall classification.
21:1.0.1.1.7.3.63.3	SECTION 7.42	7.42 Recall strategy.
21:1.0.1.1.7.3.63.4	SECTION 7.45	7.45 Food and Drug Administration-requested recall.
21:1.0.1.1.7.3.63.5	SECTION 7.46	7.46 Firm-initiated recall.
21:1.0.1.1.7.3.63.6	SECTION 7.49	7.49 Recall communications.
21:1.0.1.1.7.3.63.7	SECTION 7.50	7.50 Public notification of recall.
21:1.0.1.1.7.3.63.8	SECTION 7.53	7.53 Recall status reports.
21:1.0.1.1.7.3.63.9	SECTION 7.55	7.55 Termination of a recall.
21:1.0.1.1.7.3.63.10	SECTION 7.59	7.59 General industry guidance.

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