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
- 18,812
- Deaths
- 225
- Injuries
- 6,153
- Malfunctions
- 12,432
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
1,52626
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- System, Peritoneal, Automatic DeliveryFKX15,884
- Set, Tubing, Blood, With And Without Anti-Regurgitation ValveFJK1,385
- Set, Administration, For Peritoneal Dialysis, DisposableKDJ850
- Dialyzer, High Permeability With Or Without Sealed Dialysate SystemKDI442
- Accessories, Blood Circuit, HemodialysisKOC203
- 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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