Concord Manufacturing
FDA adverse event reports naming Concord Manufacturing as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: CONCORD MANUFACTURING.
- Total reports
- 19,794
- Deaths
- 743
- Injuries
- 4,220
- Malfunctions
- 14,831
Reports per year
313
5114
215
16916
1,46717
3,75818
3,67519
2,36420
2,53321
2,22222
1,96523
1,57024
1325
226
Source: FDA adverse event reports by year received, 2013–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- System, Peritoneal, Automatic DeliveryFKX16,533
- Dialyzer, High Permeability With Or Without Sealed Dialysate SystemKDI2,895
- Dialysate Concentrate For Hemodialysis (Liquid Or Powder)KPO258
- Accessories, Blood Circuit, HemodialysisKOC57
- Hemodialysis System For Home UseONW31
- Blender/MixerJRO15
- System, Dialysate Delivery, Single PatientFKP4
- Set, Tubing, Blood, With And Without Anti-Regurgitation ValveFJK1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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