Rice Creek Manufacturing
FDA adverse event reports naming Rice Creek Manufacturing as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: RICE CREEK MANUFACTURING.
- Total reports
- 6,385
- Deaths
- 283
- Injuries
- 3,252
- Malfunctions
- 1,947
Reports per year
72704
71105
84506
1,26507
89808
49309
35210
18111
1312
15013
115
118
319
120
121
Source: FDA adverse event reports by year received, 2004–2021. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Pump, Infusion, Implanted, ProgrammableLKK6,166
- Implantable Pacemaker Pulse-GeneratorDXY141
- Catheter, Percutaneous, Long Term, IntraspinalLNY21
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP15
- Pump, InfusionFRN13
- Catheter, Conduction, AnestheticBSO11
- Pump, Infusion, PcaMEA4
- Programmer, PacemakerKRG3
- Permanent Pacemaker ElectrodeDTB2
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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