Ogden Manufacturing Plant
FDA adverse event reports naming Ogden Manufacturing Plant as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: OGDEN MANUFACTURING PLANT.
- Total reports
- 6,188
- Deaths
- 26
- Injuries
- 340
- Malfunctions
- 5,822
Reports per year
4816
41417
50818
39719
53620
47721
64222
90323
97924
1,02825
25626
Source: FDA adverse event reports by year received, 2016–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Dialyzer, High Permeability With Or Without Sealed Dialysate SystemKDI5,889
- Dialyzer, Capillary, Hollow FiberFJI291
- Oxygenator, Cardiopulmonary BypassDTZ3
- System, Peritoneal, Automatic DeliveryFKX2
- Set, Tubing, Blood, With And Without Anti-Regurgitation ValveFJK1
- Set, Administration, For Peritoneal Dialysis, DisposableKDJ1
- Dialysate Concentrate For Hemodialysis (Liquid Or Powder)KPO1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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