Government Report: Medical Devices: FDA Should Enhance Its Oversight of Recalls

July 26, 2011 at 8:00 am Leave a comment

Medical Devices: FDA Should Enhance Its Oversight of Recalls

by Marcia Crosse
Paperback, 57 pages, 2011, $25.00
ISBN: 1437988067

Recalls are an important tool to mitigate serious health consequences associated with defective or unsafe medical devices. Typically, a recall is voluntarily initiated by the firm that manufactured the device. The FDA oversees implementation of the recall. FDA classifies recalls based on health risks of using the recalled device. FDA also determines whether a firm has effectively implemented a recall, and when a recall can be terminated.

This report identifies: (1) the numbers and characteristics of medical device recalls and FDA’s use of this info. to aid its oversight; and (2) the extent to which the process ensures the effective implementation and termination of the highest-risk recalls. Charts and tables. A print on demand report.

Purchase this print-on-demand publication for $25.00:

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