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Philips Goldway (shenzhen) Industrial Inc

FDA adverse event reports naming Philips Goldway (shenzhen) Industrial Inc as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: PHILIPS GOLDWAY (SHENZHEN) INDUSTRIAL INC.

Total reports
3,532
Deaths
14
Injuries
51
Malfunctions
3,467

Reports per year

21
22
23

Source: FDA adverse event reports by year received, 20212023. 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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