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074 a| 0546-D (online);

086 0 a| GA 1.13:GAO-26-107619;

088 a| GAO-26-107619;

110 1 a| United States.b| Government Accountability Office,e| author.=| ^A580995;

245 10 a| Medical device recalls: HHS and FDA should address limitations in oversight of recall process :b| report to congressional requesters.;

246 3 a| Medical device recalls: Health and Human Services and Food and Drug Administration should address limitations in oversight of recall process, report to congressional requesters;

264 1 a| Washington, DC :b| United States Government Accountability Office,c| 2025.;

300 a| 1 online resource (ii, 44 pages) :b| color illustrations;

336 a| textb| txt2| rdacontent;

337 a| computerb| c2| rdamedia;

338 a| online resourceb| cr2| rdacarrier;

500 a| December 2025;

500 a| "GAO-26-107619.";

500 a| This is a publication issued by the United States federal government or produced with federal funds.;

500 a| In scope of the U.S. Government Publishing Office Cataloging and Indexing Program (C&I) and Federal Depository Library Program (FDLP).;

504 a| Includes bibliographical references.;

588 a| Description based on online resource; title from PDF cover (GAO, viewed December 16, 2025).;

610 10 a| United States.b| Department of Health and Human Services.=| ^A11611;

610 10 a| United States.b| Food and Drug Administration.=| ^A1253;

650 0 a| Product recallz| United States.=| ^A1013677;

650 0 a| Medical instruments and apparatusx| Safety regulationsz| United States.=| ^A420502;

856 40 u| https://purl.fdlp.gov/GPO/gpo2510617| 0;

856 4 z| Address at time of PURL creationu| https://www.gao.gov/assets/gao-26-107619.pdf;

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999 a| CLICK ON WEB ADDRESSw| ASISc| 1i| 6698723-1001l| JNETm| JOYNERr| Ys| Yt| JNE1DOu| 1/22/2026x| EDOCUMENTz| JERESOURCEo| .STAFF. jjlm;

Medical device recalls: HHS and FDA should address limitations in oversight of recall process : report to congressional requesters.

Author/creator	United States
Format	Electronic
Publication	Washington, DC : United States Government Accountability Office, 2025.
Description	1 online resource (ii, 44 pages) : color illustrations
Supplemental Content	https://purl.fdlp.gov/GPO/gpo251061
Supplemental Content	Address at time of PURL creation
Subjects	United States. Department of Health and Human Services. United States. Food and Drug Administration. Product recall--United States. Medical instruments and apparatus--Safety regulations. --United States.

Variant title	Medical device recalls: Health and Human Services and Food and Drug Administration should address limitations in oversight of recall process, report to congressional requesters
General note	December 2025
General note	"GAO-26-107619."
General note	This is a publication issued by the United States federal government or produced with federal funds.
General note	In scope of the U.S. Government Publishing Office Cataloging and Indexing Program (C&I) and Federal Depository Library Program (FDLP).
Bibliography note	Includes bibliographical references.
Source of description	Description based on online resource; title from PDF cover (GAO, viewed December 16, 2025).
Technical rpt number	GAO-26-107619
GPO item number	0546-D (online)
Govt. docs number	GA 1.13:GAO-26-107619

Availability

Library	Location	Call Number	Status	Item Actions
	Electronic Resources	Online Content https://purl.fdlp.gov/GPO/gpo251061 Address at time of PURL creation	✔ Available

Medical device recalls: HHS and FDA should address limitations in oversight of recall process : report to congressional requesters.

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