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Steris Mexico, S. DE R.L. DE C.V.

FDA adverse event reports naming Steris Mexico, S. DE R.L. DE C.V. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STERIS MEXICO, S. DE R.L. DE C.V..

Total reports
1,409
Deaths
0
Injuries
29
Malfunctions
814

Reports per year

12
13
14
15
16
17
18
19
20
21
22
23
24
25
26

Source: FDA adverse event reports by year received, 2012–2026. 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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