Availability of Unique Device Identifiers for Class I Medical Device Recalls From 2018 to 2022.

Mooghali, Maryam; Ross, Joseph S; Kadakia, Kushal T; Dhruva, Sanket S

Mooghali, Maryam; Ross, Joseph S; Kadakia, Kushal T; Dhruva, Sanket S.

Afiliación

Mooghali M; Section of General Internal Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.
Ross JS; Yale Collaboration for Regulatory Rigor, Integrity, and Transparency, Yale School of Medicine, New Haven, Connecticut.
Kadakia KT; Section of General Internal Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.
Dhruva SS; Yale Collaboration for Regulatory Rigor, Integrity, and Transparency, Yale School of Medicine, New Haven, Connecticut.

JAMA Intern Med ; 183(7): 735-737, 2023 07 01.

Article en En | MEDLINE | ID: mdl-37184854

This cross-sectional study describes the inclusion of unique device identifier in recall notices for moderate- and high-risk medical devices in the US.

Asunto(s)

Aprobación de Recursos; Recall de Suministro Médico; Humanos; Estados Unidos; Factores de Riesgo; United States Food and Drug Administration; Vigilancia de Productos Comercializados

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Aprobación de Recursos / Recall de Suministro Médico Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: JAMA Intern Med Año: 2023 Tipo del documento: Article Pais de publicación: Estados Unidos

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