[Code of Federal Regulations]
[Title 21, Volume 1]
[Revised as of April 1, 2002]
From the U.S. Government Printing Office via GPO Access
[CITE: 21CFR5.411]

[Page 60]
 
                        TITLE 21--FOOD AND DRUGS
 
CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN 
                                SERVICES
 
PART 5--DELEGATIONS OF AUTHORITY AND ORGANIZATION--Table of Contents
 
  Subpart F--Medical Devices and Radiological Health; Redelegations of 
                                Authority
 
Sec. 5.411  Medical device recall authority.

    (a) The following officials, for medical devices assigned to their 
respective organizations, are authorized to perform all of the recall 
functions under section 518(e) of the Federal Food, Drug, and Cosmetic 
Act (21 U.S.C. 360h(e)), which have been delegated to the Commissioner 
of Food and Drugs:
    (1) The Director and Deputy Directors for Science and for 
Regulations and Policy, Center for Devices and Radiological Health 
(CDRH).
    (2) The Director and Deputy Director, Office of Compliance, CDRH.
    (3) The Director, the Deputy Director, and the Directors, Office of 
Review Management and Office of Pharmaceutical Science, Center for Drug 
Evaluation and Research (CDER); and the Director and Deputy Director, 
Office of Compliance, CDER.
    (4) The Director and Deputy Directors, Center for Biologics 
Evaluation and Research (CBER), and the Director and Deputy Directors, 
Office of Compliance and Biologics Quality, CBER.
    (b) These officials may not further redelegate this authority.