Erika DE Reynosa, S.A. DE C.V.
FDA adverse event reports naming Erika DE Reynosa, S.A. DE C.V. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ERIKA DE REYNOSA, S.A. DE C.V..
- Total reports
- 19,357
- Deaths
- 229
- Injuries
- 6,299
- Malfunctions
- 12,826
Reports per year
512
1913
514
915
11016
1,18617
2,08818
1,96619
1,92220
1,92421
1,77622
1,49623
1,64624
3,13025
2,07126
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- System, Peritoneal, Automatic DeliveryFKX16,113
- Set, Tubing, Blood, With And Without Anti-Regurgitation ValveFJK1,680
- Set, Administration, For Peritoneal Dialysis, DisposableKDJ855
- Dialyzer, High Permeability With Or Without Sealed Dialysate SystemKDI457
- Accessories, Blood Circuit, HemodialysisKOC204
- Dialysate Concentrate For Hemodialysis (Liquid Or Powder)KPO28
- Hemodialysis System For Home UseONW12
- Product code ------2
- Protector, Transducer, DialysisFIB2
- Autonomous Extracorporeal Blood Leak Detector/AlarmODX2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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