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
- 6,359
- Deaths
- 283
- Injuries
- 3,235
- Malfunctions
- 1,949
Reports per year
72704
70505
83906
1,25407
89808
49209
35210
18011
1312
15013
115
118
319
120
121
Source: FDA adverse event reports by year received, 2004–2021. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Pump, Infusion, Implanted, ProgrammableLKK6,140
- 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.
Monitor Rice Creek Manufacturing automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.