Liebel-flarsheim Co.
FDA adverse event reports naming Liebel-flarsheim Co. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: LIEBEL-FLARSHEIM CO..
- Total reports
- 1,220
- Deaths
- 6
- Injuries
- 234
- Malfunctions
- 902
Reports per year
1399
200
101
1603
2104
1505
1606
1407
19408
20309
13710
21611
17412
15113
714
Source: FDA adverse event reports by year received, 1999–2014. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Table, Cystometric, Non-Electric And AccessoriesKQS525
- Injector And Syringe, AngiographicDXT287
- Table, Radiographic, TiltingIXR223
- Injector, Contrast Medium, AutomaticIZQ167
- Table And Attachments, Operating-RoomBWN3
- Table, Operating-Room, Ac-PoweredFQO2
- Table, Cystometric, ElectricMMZ2
- Tubing, Pressure And AccessoriesBYX1
- Catheter, Flow DirectedDYG1
- Table, Cysto, Non-ElectricalEYH1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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