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Quickie Designs, Inc.

FDA adverse event reports naming Quickie Designs, Inc. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: QUICKIE DESIGNS, INC..

Total reports
1,969
Deaths
1
Injuries
10
Malfunctions
1,955

Reports per year

95
96
97
98

Source: FDA adverse event reports by year received, 19951998. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.

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Recent recalls

No recalls listed in the FDA device recall database for this entry.

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