[Code of Federal Regulations]
[Title 16, Volume 2]
[Revised as of January 1, 2005]
From the U.S. Government Printing Office via GPO Access
[CITE: 16CFR1115.20]

[Page 169-172]
 
                     TITLE 16--COMMERCIAL PRACTICES
 
             CHAPTER II--CONSUMER PRODUCT SAFETY COMMISSION
 
PART 1115_SUBSTANTIAL PRODUCT HAZARD REPORTS--Table of Contents
 
                Subpart B_Remedial Actions and Sanctions
 
Sec. 1115.20  Voluntary remedial actions.


    As appropriate, the Commission will attempt to protect the public 
from substantial product hazards by seeking one or more of the following 
voluntary remedies:
    (a) Corrective action plans. A corrective action plan is a document, 
signed by a subject firm, which sets forth the remedial action which the 
firm will voluntarily undertake to protect the public, but which has no 
legally binding effect. The Commission reserves

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the right to seek broader corrective action if it becomes aware of new 
facts or if the corrective action plan does not sufficiently protect the 
public.
    (1) Corrective action plans shall include, as appropriate:
    (i) A statement of the nature of the alleged hazard associated with 
the product, including the nature of the alleged defect or noncompliance 
and type(s) of injury or potential injury presented.
    (ii) A detailed statement of the means to be employed to notify the 
public of the alleged product hazard (e.g., letter, press release, 
advertising), including an identification of the classes of persons who 
will receive such notice and a copy or copies of the notice or notices 
to be used.
    (iii) A specification of model number and/or other appropriate 
descriptions of the product.
    (iv) Any necessary instructions regarding use or handling of the 
product pending correction.
    (v) An explanation of the specific cause of the alleged substantial 
product hazard, if known.
    (vi) A statement of the corrective action which will be or has been 
taken to eliminate the alleged substantial product hazard. The firm 
should indicate whether it is repairing or replacing the product or 
refunding its purchase price. If products are to be returned to a 
subject firm, the corrective action plan should indicate their 
disposition (e.g., reworked, destroyed, returned to foreign 
manufacturer). Samples of replacement products and relevant drawings and 
test data for repairs or replacements should be available.
    (vii) A statement of the steps that will be, or have been, taken to 
reasonably prevent recurrence of the alleged substantial product hazard 
in the future.
    (viii) A statement of the action which will be undertaken to correct 
product units in the distribution chain, including a timetable and 
specific information about the number and location of such units.
    (ix) The signatures of representatives of the subject firm.
    (x) An acknowledgment by the subject firm that the Commission may 
monitor the corrective action and that the firm will furnish necessary 
information, including customer lists.
    (xi) An agreement that the Commission may publicize the terms of the 
plan to the extent necessary to inform the public of the nature and 
extent of the alleged substantial product hazard and of the actions 
being undertaken to correct the alleged hazard presented.
    (xii) Additional points of agreement, as appropriate.
    (xiii) If desired by the subject firm, the following statement or 
its equivalent: ``The submission of this corrective action plan does not 
constitute an admission by (the subject firm) that either reportable 
information or a substantial product hazard exists.''
    (xiv) An acknowledgment that the corrective action plan becomes 
effective only upon its final acceptance by the Commission.
    (2) In determining whether to recommend to the Commission acceptance 
of a corrective action plan, the staff shall consider favorably both the 
promptness of the subject firm's reporting and any remedial actions 
taken by the subject firm in the interest of public safety. The staff 
also shall consider, insofar as possible, prior involvement by the 
subject firm in corrective action plans and Commission orders if such 
involvement bears on the likelihood that the firm will comply fully with 
the terms of the corrective action plan.
    (3) Upon receipt of a corrective action plan and staff 
recommendation, the Commission may:
    (i) Approve the plan;
    (ii) Reject the plan and issue a complaint (in which case an 
administrative and/or judicial proceeding will be commenced); or
    (iii) Take any other action necessary to insure that the plan is 
adequate.
    (4) When time permits and where practicable in the interest of 
protecting the public, a summary of the plan shall be published in the 
Commission's Public Calendar. Those portions of the plan that are not 
restricted will be made available to the public in the Commission's 
public reading room as much in advance of the Commission meeting as 
practicable. Any interested person wishing to comment on the plan

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must file a Notice of Intent to Comment at least forty-eight (48) hours 
prior to the commencement of the Commission meeting during which the 
plan will be discussed. If no notices of intent are received, the 
Commission may take final action on the plan. If such notice is received 
within the time limits detailed above, the plan will, if practicable, be 
docketed for the following week's agenda. All comments must be in 
writing, and final written comments must be submitted at least forty-
eight (48) hours before that session.
    (b) Consent order agreements under section 15 of CPSA. The consent 
order agreement (agreement) is a document executed by a subject firm 
(Consenting Party) and a Commission staff representative which 
incorporates both a proposed complaint setting forth the staff's charges 
and a proposed order by which such charges are resolved.
    (1) Consent order agreements shall include, as appropriate:
    (i) An admission of all jurisdictional facts by the Consenting 
Party.
    (ii) A waiver of any rights to an administrative or judicial hearing 
and of any other procedural steps, including any rights to seek judicial 
review or otherwise challenge or contest the validity of the 
Commission's Order.
    (iii) A statement that the agreement is in settlement of the staff's 
charges.
    (iv) A statement that the Commission's Order is issued under section 
15 of the CPSA (15 U.S.C. 2064) and that a violation is a prohibited act 
within the meaning of section 19(a)(5) of the CPSA (15 U.S.C. 
2068(a)(5)) and may subject a violator to civil and/or criminal 
penalties under sections 20 and 21 of the CPSA (15 U.S.C. 2069 and 
2070).
    (v) An acknowledgment that the Commission reserves its right to seek 
sanctions for any violations of the reporting obligations of section 
15(b) of CPSA (15 U.S.C. 2064(b)) and its right to take other 
appropriate legal action.
    (vi) An acknowledgment that the agreement becomes effective only 
upon its final acceptance by the Commission and its service upon the 
Consenting Party.
    (vii) An acknowledgment that the Commission may disclose terms of 
the consent order agreement to the public.
    (viii) A listing of the acts or practices from which the Consenting 
Party will refrain.
    (ix) A statement that the Consenting Party shall perform certain 
acts and practices pursuant to the agreement.
    (x) An acknowledgment that any interested person may bring an action 
pursuant to section 24 of the CPSA (15 U.S.C. 2073) in any U.S. district 
court for the district in which the Consenting Party is found or 
transacts business to enforce the order and to obtain appropriate 
injunctive relief.
    (xi) A description of the alleged substantial product hazard.
    (xii) If desired by the Consenting Party, the following statement or 
its equivalent: ``The signing of this consent order agreement does not 
constitute an admission by (the Consenting Party) that either reportable 
information or a substantial product hazard exists.''
    (xiii) The elements of a corrective action plan as set forth in 
Sec. 1115.20(a).
    (2) At any time in the course of an investigation, the staff may 
propose to a subject firm which is being investigated that some or all 
of the allegations be resolved by a consent order agreement. 
Additionally, such a proposal may be made to the staff by a subject 
firm.
    (3) Upon receiving an executed agreement, the Commission may:
    (i) Provisionally accept it;
    (ii) Reject it and issue a complaint (in which case an 
administrative and/or judicial proceeding will be commenced); or
    (iii) Take such other action as it may deem appropriate.
    (4) If the consent order agreement is provisionally accepted, the 
Commission shall place the agreement on the public record and shall 
announce provisional acceptance of the agreement in the Commission's 
public calendar and in the Federal Register. Any interested person may 
request the Commission not to accept the agreement by filing a written 
request in the Office of the Secretary. Such written request must be 
received in the Office of the Secretary no later than the close of 
business of the fifteenth (15th) calendar day following the date of 
announcement in the Federal Register.

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    (5) If the Commission does not receive any requests not to accept 
the agreement within the time period specified above, the consent order 
agreement shall be deemed finally accepted by the Commission on the 
twentieth (20th) calendar day after the date of announcement in the 
Federal Register, unless the Commission determines otherwise. However, 
if the Commission does receive a request not to accept the consent order 
agreement, then it will consider such request and vote on the 
acceptability of such agreement or the desirability of further action. 
After the consent order agreement is finally accepted, the Commission 
may then issue its complaint and order in such form as the circumstances 
may require. The order is a final order in disposition of the proceeding 
and is effective immediately upon its service upon the Consenting Party 
pursuant to the Commission's Rules of Practice for Adjudicative 
Proceedings (16 CFR part 1025). The Consenting Party shall thereafter be 
bound by and take immediate action in accordance with such final order.
    (6) If the Commission does not accept the consent order agreement on 
a final basis, it shall so notify the Consenting Party. Such 
notification constitutes withdrawal of the Commission's provisional 
acceptance unless the Commission orders otherwise. The Commission then 
may:
    (i) Issue a complaint, in which case an administrative and/or 
judicial proceeding will be commenced;
    (ii) Order further investigation; or
    (iii) Take such other action as it may deem appropriate.