Reynosa Manufacturing
FDA adverse event reports naming Reynosa Manufacturing as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: REYNOSA MANUFACTURING.
- Total reports
- 2,089
- Deaths
- 39
- Injuries
- 217
- Malfunctions
- 1,823
Reports per year
2301
1702
9803
5004
4405
11006
6207
4008
3809
10410
24511
28212
53713
40714
3215
Source: FDA adverse event reports by year received, 2001–2015. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- System, Peritoneal, Automatic DeliveryFKX1,326
- Set, Tubing, Blood, With And Without Anti-Regurgitation ValveFJK463
- Set, Administration, For Peritoneal Dialysis, DisposableKDJ145
- Accessories, Blood Circuit, HemodialysisKOC110
- Filter, Blood, DialysisFKJ21
- ClampHXD8
- Dialyzer, High Permeability With Or Without Sealed Dialysate SystemKDI4
- Lithotriptor, Extracorporeal Shock-Wave, UrologicalLNS3
- Hemodialysis System For Home UseONW2
- Catheter, Cannula And Tubing, Vascular, Cardiopulmonary BypassDWF1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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