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Hill-rom DE Mexico S DE RL DE CV

FDA adverse event reports naming Hill-rom DE Mexico S DE RL DE CV as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: HILL-ROM DE MEXICO S DE RL DE CV.

Total reports
1,170
Deaths
0
Injuries
8
Malfunctions
1,126

Reports per year

10
11
12
13
14
15

Source: FDA adverse event reports by year received, 20102015. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.

Top device categories

Recent recalls

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

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