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21 U.S.C. § 350l — Mandatory recall authority

Federal law — U.S. Code and appendices · legal_authorities

21 U.S.C. § 350l — Mandatory recall authority

**(a) Voluntary procedures** If the Secretary determines, based on information gathered through the reportable food registry under [section 350f of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section350f&num=0&edition=prelim) or through any other means, that there is a reasonable probability that an article of food (other than infant formula) is adulterated under [section 342 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section342&num=0&edition=prelim) or misbranded under [section 343(w) of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section343/w&num=0&edition=prelim) and the use of or exposure to such article will cause serious adverse health consequences or death to humans or animals, the Secretary shall provide the responsible party (as defined in [section 350f of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section350f&num=0&edition=prelim)) with an opportunity to cease distribution and recall such article. **(b) Prehearing order to cease distribution and give notice** (1) **In general** — If the responsible party refuses to or does not voluntarily cease distribution or recall such article within the time and in the manner prescribed by the Secretary (if so prescribed), the Secretary may, by order require, as the Secretary deems necessary, such person to— (A) immediately cease distribution of such article; and (B) as applicable, immediately notify all persons— (i) manufacturing, processing, packing, transporting, distributing, receiving, holding, or importing and selling such article; and (ii) to which such article has been distributed, transported, or sold, to immediately cease distribution of such ar

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Stable record: federal_law:legal_authorities:record_usc_528f63dfe3d2815c1d27a29d
Source file: Laws/federal/codes/united-states-code/title-21/section-350l-mandatory-recall-authority--48f7925db0.md
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Source location: Title 21, Chapter 9, § 350l; chapter-009-federal-food-drug-and-cosmetic-act.md

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**(a) Voluntary procedures** If the Secretary determines, based on information gathered through the reportable food registry under [section 350f of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section350f&num=0&edition=prelim) or through any other means, that there is a reasonable probability that an article of food (other than infant formula) is adulterated under [section 342 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section342&num=0&edition=prelim) or misbranded under [section 343(w) of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section343/w&num=0&edition=prelim) and the use of or exposure to such article will cause serious adverse health consequences or death to humans or animals, the Secretary shall provide the responsible party (as defined in [section 350f of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section350f&num=0&edition=prelim)) with an opportunity to cease distribution and recall such article. **(b) Prehearing order to cease distribution and give notice** (1) **In general** — If the responsible party refuses to or does not voluntarily cease distribution or recall such article within the time and in the manner prescribed by the Secretary (if so prescribed), the Secretary may, by order require, as the Secretary deems necessary, such person to— (A) immediately cease distribution of such article; and (B) as applicable, immediately notify all persons— (i) manufacturing, processing, packing, transporting, distributing, receiving, holding, or importing and selling such article; and (ii) to which such article has been distributed, transported, or sold, to immediately cease distribution of such article.11 So in original. The words “to immediately cease distribution of such article.” probably should follow cl. (ii). (2) **Required additional information** (A) *In general* — If an article of food covered by a recall order issued under paragraph (1)(B) has been distributed to a warehouse-based third party logistics provider without providing such provider sufficient information to know or reasonably determine the precise identity of the article of food covered by a recall order that is in its possession, the notice provided by the responsible party subject to the order issued under paragraph (1)(B) shall include such information as is necessary for the warehouse-based third party logistics provider to identify the food. (B) *Rules of construction* — Nothing in this paragraph shall be construed— (i) to exempt a warehouse-based third party logistics provider from the requirements of this chapter, including the requirements in this section and [section 350c of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section350c&num=0&edition=prelim); or (ii) to exempt a warehouse-based third party logistics provider from being the subject of a mandatory recall order. (3) **Determination to limit areas affected** — If the Secretary requires a responsible party to cease distribution under paragraph (1)(A) of an article of food identified in subsection (a), the Secretary may limit the size of the geographic area and the markets affected by such cessation if such limitation would not compromise the public health. **(c) Hearing on order** The Secretary shall provide the responsible party subject to an order under subsection (b) with an opportunity for an informal hearing, to be held as soon as possible, but not later than 2 days after the issuance of the order, on the actions required by the order and on why the article that is the subject of the order should not be recalled. **(d) Post-hearing recall order and modification of order** (1) **Amendment of order** — If, after providing opportunity for an informal hearing under subsection (c), the Secretary determines that removal of the article from commerce is necessary, the Secretary shall, as appropriate— (A) amend the order to require recall of such article or other appropriate action; (B) specify a timetable in which the recall shall occur; (C) require periodic reports to the Secretary describing the progress of the recall; and (D) provide notice to consumers to whom such article was, or may have been, distributed. (2) **Vacating of order** — If, after such hearing, the Secretary determines that adequate grounds do not exist to continue the actions required by the order, or that such actions should be modified, the Secretary shall vacate the order or modify the order. **(e) Rule regarding alcoholic beverages** The Secretary shall not initiate a mandatory recall or take any other action under this section with respect to any alcohol beverage until the Secretary has provided the Alcohol and Tobacco Tax and Trade Bureau with a reasonable opportunity to cease distribution and recall such article under the Alcohol and Tobacco Tax and Trade Bureau authority. **(f) Cooperation and consultation** The Secretary shall work with State and local public health officials in carrying out this section, as appropriate. **(g) Public notification** In conducting a recall under this section, the Secretary shall— (1) ensure that a press release is published regarding the recall, as well as alerts and public notices, as appropriate, in order to provide notification— (A) of the recall to consumers and retailers to whom such article was, or may have been, distributed; and (B) that includes, at a minimum— (i) the name of the article of food subject to the recall; (ii) a description of the risk associated with such article; and (iii) to the extent practicable, information for consumers about similar articles of food that are not affected by the recall; (2) consult the policies of the Department of Agriculture regarding providing to the public a list of retail consignees receiving products involved in a Class I recall and shall consider providing such a list to the public, as determined appropriate by the Secretary; and (3) if available, publish on the Internet Web site of the Food and Drug Administration an image of the article that is the subject of the press release described in (1).22 So in original. Probably should be “paragraph (1).” **(h) No delegation** The authority conferred by this section to order a recall or vacate a recall order shall not be delegated to any officer or employee other than the Commissioner. **(i) Effect** Nothing in this section shall affect the authority of the Secretary to request or participate in a voluntary recall, or to issue an order to cease distribution or to recall under any other provision of this chapter or under the Public Health Service Act [[42 U.S.C. 201](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title42-section201&num=0&edition=prelim) et seq.]. **(j) Coordinated communication** (1) **In general** — To assist in carrying out the requirements of this subsection, the Secretary shall establish an incident command operation or a similar operation within the Department of Health and Human Services that will operate not later than 24 hours after the initiation of a mandatory recall or the recall of an article of food for which the use of, or exposure to, such article will cause serious adverse health consequences or death to humans or animals. (2) **Requirements** — To reduce the potential for miscommunication during recalls or regarding investigations of a food borne illness outbreak associated with a food that is subject to a recall, each incident command operation or similar operation under paragraph (1) shall use regular staff and resources of the Department of Health and Human Services to— (A) ensure timely and coordinated communication within the Department, including enhanced communication and coordination between different agencies and organizations within the Department; (B) ensure timely and coordinated communication from the Department, including public statements, throughout the duration of the investigation and related foodborne illness outbreak; (C) identify a single point of contact within the Department for public inquiries regarding any actions by the Secretary related to a recall; (D) coordinate with Federal, State, local, and tribal authorities, as appropriate, that have responsibilities related to the recall of a food or a foodborne illness outbreak associated with a food that is subject to the recall, including notification of the Secretary of Agriculture and the Secretary of Education in the event such recalled food is a commodity intended for use in a child nutrition program (as identified in [section 1769f(b) of title 42](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title42-section1769f/b&num=0&edition=prelim)); and (E) conclude operations at such time as the Secretary determines appropriate. (3) **Multiple recalls** — The Secretary may establish multiple or concurrent incident command operations or similar operations in the event of multiple recalls or foodborne illness outbreaks necessitating such action by the Department of Health and Human Services.

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Federal law — U.S. Code and appendices · legal_authorities

21 U.S.C. § 350f — Reportable food registry

**(a) Definitions** In this section: (1) **Responsible party** — The term “responsible party”, with respect to an article of food, means a person that submits the registration under [section 350d(a) of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section350d/a&num=0&edition=prelim) for a food facility that is required to register under [section 350d(a) of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section350d/a&num=0&edition=prelim), at which such article of food is manufactured, processed, packed, or held. (2) **Reportable food** — The term “reportable food” means an article of food (other than infant formula) for which there is a reasonable probability that the use of, or exposure to, such article of food will cause serious adverse health consequences or death to humans or animals. **(b) Establishment** (1) **In general** — Not later than 1 year after September 27, 2007, the Secretary shall establish within the Food and Drug Administration a Reportable Food Registry to which instances of reportable food may be submitted by the Food and Drug Administration after receipt of reports under subsection (d), via an electronic portal, from— (A) Federal, State, and local public health officials; or (B) responsible parties. (2) **Review by Secretary** — The Secretary shall promptly review and assess the information submitted under paragraph (1) for the purposes of identifying reportable food, submitting entries to the Reportable Food Registry, acting under subsection (c), and exercising other existing food safety authorities under this chapter to protect the public health. **(c) Issuance of an alert by the Secretary** (1) **In general** — The Secretary shall issue, or cause to be issued, an a

Source: Supplied U.S. Code snapshot — release unconfirmed · 21 U.S.C. § 350f

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Federal law — U.S. Code and appendices · legal_authorities

21 U.S.C. § 350 — Vitamins and minerals

**(a) Authority and limitations of Secretary; applicability** (1) Except as provided in paragraph (2)— (A) the Secretary may not establish, under section 321(n), 341, or 343 of this title, maximum limits on the potency of any synthetic or natural vitamin or mineral within a food to which this section applies; (B) the Secretary may not classify any natural or synthetic vitamin or mineral (or combination thereof) as a drug solely because it exceeds the level of potency which the Secretary determines is nutritionally rational or useful; (C) the Secretary may not limit, under section 321(n), 341, or 343 of this title, the combination or number of any synthetic or natural— (i) vitamin, (ii) mineral, or (iii) other ingredient of food, within a food to which this section applies. (2) Paragraph (1) shall not apply in the case of a vitamin, mineral, other ingredient of food, or food, which is represented for use by individuals in the treatment or management of specific diseases or disorders, by children, or by pregnant or lactating women. For purposes of this subparagraph,11 So in original. Probably should be “paragraph”. the term “children” means individuals who are under the age of twelve years. **(b) Labeling and advertising requirements for foods** (1) A food to which this section applies shall not be deemed under [section 343 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section343&num=0&edition=prelim) to be misbranded solely because its label bears, in accordance with [section 343(i)(2) of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section343/i/2&num=0&edition=prelim), all the ingredients in the food or its advertising contains references to ingredients in the food

Source: Supplied U.S. Code snapshot — release unconfirmed · 21 U.S.C. § 350

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Federal law — U.S. Code and appendices · legal_authorities

21 U.S.C. § 350c — Maintenance and inspection of records

**(a) Records inspection** (1) **Adulterated food** — If the Secretary has a reasonable belief that an article of food, and any other article of food that the Secretary reasonably believes is likely to be affected in a similar manner, is adulterated and presents a threat of serious adverse health consequences or death to humans or animals, each person (excluding farms and restaurants) who manufactures, processes, packs, distributes, receives, holds, or imports such article shall, at the request of an officer or employee duly designated by the Secretary, permit such officer or employee, upon presentation of appropriate credentials and a written notice to such person, at reasonable times and within reasonable limits and in a reasonable manner, to have access to and copy all records relating to such article, and to any other article of food that the Secretary reasonably believes is likely to be affected in a similar manner, that are needed to assist the Secretary in determining whether the food is adulterated and presents a threat of serious adverse health consequences or death to humans or animals. (2) **Use of or exposure to food of concern** — If the Secretary believes that there is a reasonable probability that the use of or exposure to an article of food, and any other article of food that the Secretary reasonably believes is likely to be affected in a similar manner, will cause serious adverse health consequences or death to humans or animals, each person (excluding farms and restaurants) who manufactures, processes, packs, distributes, receives, holds, or imports such article shall, at the request of an officer or employee duly designated by the Secretary, permit such officer or employee, upon presentation of appropriate credentials and a written notice to such pe

Source: Supplied U.S. Code snapshot — release unconfirmed · 21 U.S.C. § 350c

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Federal law — U.S. Code and appendices · legal_authorities

42 U.S.C. § 201 — Funding

Beginning with fiscal year 2010, the Secretary shall transfer from the Public Health and Social Services Emergency Fund such sums as may be necessary to carry out this part.

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Federal law — U.S. Code and appendices · legal_authorities

21 U.S.C. § 342 — Adulterated food

A food shall be deemed to be adulterated— **(a) Poisonous, insanitary, etc., ingredients** (1) If it bears or contains any poisonous or deleterious substance which may render it injurious to health; but in case the substance is not an added substance such food shall not be considered adulterated under this clause if the quantity of such substance in such food does not ordinarily render it injurious to health.11 So in original. The period probably should be “; or”. (2)(A) if it bears or contains any added poisonous or added deleterious substance (other than a substance that is a pesticide chemical residue in or on a raw agricultural commodity or processed food, a food additive, a color additive, or a new animal drug) that is unsafe within the meaning of [section 346 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section346&num=0&edition=prelim); or (B) if it bears or contains a pesticide chemical residue that is unsafe within the meaning of [section 346a(a) of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section346a/a&num=0&edition=prelim); or (C) if it is or if it bears or contains (i) any food additive that is unsafe within the meaning of [section 348 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section348&num=0&edition=prelim); or (ii) a new animal drug (or conversion product thereof) that is unsafe within the meaning of [section 360b of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section360b&num=0&edition=prelim); or (3) if it consists in whole or in part of any filthy, putrid, or decomposed substance, or if it is otherwise unfit for food; or (4) if it has been prepared, packed, or held under insanitary conditions wher

Source: Supplied U.S. Code snapshot — release unconfirmed · 21 U.S.C. § 342

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Federal law — U.S. Code and appendices · legal_authorities

21 U.S.C. § 350l — Mandatory recall authority

Page 152 TITLE 21—FOOD AND DRUGS § 350l niques are followed and reports of analyses are certified as true and accurate; (ii) internal quality systems are estab- lished and maintained; (iii) procedures exist to evaluate and re- spond promptly to complaints regarding analyses and other activities for which the laboratory is accredited; and (iv) individuals who conduct the sam- pling and analyses are qualified by train- ing and experience to do so; and (B) any other criteria determined appro- priate by the Secretary. (7) Review of recognition To ensure compliance with the requirements of this section, the Secretary— (A) shall periodically, and in no case less than once every 5 years, reevaluate accredi- tation bodies recognized under paragraph (1) and may accompany auditors from an ac- creditation body to assess whether the ac- creditation body meets the criteria for rec- ognition; and (B) shall promptly revoke the recognition of any accreditation body found not to be in compliance with the requirements of this section, specifying, as appropriate, any terms and conditions necessary for labora- tories accredited by such body to continue to perform testing as described in this sec- tion. (b) Testing procedures (1) In general Not later than 30 months after January 4, 2011, food testing shall be conducted by Fed- eral laboratories or non-Federal laboratories that have been accredited for the appropriate sampling or analytical testing methodology or methodologies by a recognized accreditation body on the registry established by the Sec- retary under subsection (a)(1)(B) whenever such testing is conducted— (A) by or on behalf of an owner or con- signee— (i) in response to a specific testing re- quirement under this chapter or imple- menting regulations

Source: Supplied 2024 U.S. Code historical extraction · 21 U.S.C. § 350l

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Federal law — U.S. Code and appendices · legal_authorities

42 U.S.C. § 201 — Definitions

Page 35 TITLE 42—THE PUBLIC HEALTH AND WELFARE § 201 1 See References in Text note below. Sec. 300jj–34. Competitive grants to States and Indian tribes for the development of loan pro- grams to facilitate the widespread adoption of certified EHR technology. 300jj–35. Demonstration program to integrate in- formation technology into clinical education. 300jj–36. Information technology professionals in health care. 300jj–37. General grant and loan provisions. 300jj–38. Authorization for appropriations. PART C—OTHER PROVISIONS 300jj–51. Health information technology enroll- ment standards and protocols. 300jj–52. Information blocking. SUBCHAPTER XXIX—DATA COLLECTION, ANALYSIS, AND QUALITY 300kk. Data collection, analysis, and quality. SUBCHAPTER XXX—COMMUNITY LIVING ASSISTANCE SERVICES AND SUPPORTS 300ll to 300ll–9. Repealed. SUBCHAPTER XXXI—WORLD TRADE CENTER HEALTH PROGRAM PART A—ESTABLISHMENT OF PROGRAM; ADVISORY COMMITTEE 300mm. Establishment of World Trade Center Health Program. 300mm–1. WTC Health Program Scientific/Tech- nical Advisory Committee; WTC Health Program Steering Committees. 300mm–2. Education and outreach. 300mm–3. Uniform data collection and analysis. 300mm–4. Clinical Centers of Excellence and Data Centers. 300mm–5. Definitions. PART B—PROGRAM OF MONITORING, INITIAL HEALTH EVALUATIONS, AND TREATMENT SUBPART 1—WTC RESPONDERS 300mm–21. Identification of WTC responders and provision of WTC-related monitoring services. 300mm–22. Treatment of enrolled WTC responders for WTC-related health conditions. 300mm–23. National arrangement for benefits for el- igible individuals outside New York. SUBPART 2—WTC SURVIVORS 300mm–31. Identification and initial health evalua- tion of screening-eligible and

Source: Supplied 2024 U.S. Code historical extraction · 42 U.S.C. § 201

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