Rice Creek MFG
FDA adverse event reports naming Rice Creek MFG as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: RICE CREEK MFG.
- Total reports
- 4,335
- Deaths
- 98
- Injuries
- 2,249
- Malfunctions
- 1,851
Reports per year
5811
41912
1,76213
24914
23015
14216
10917
9818
11119
20620
721
122
224
525
126
Source: FDA adverse event reports by year received, 2011–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Pump, Infusion, Implanted, ProgrammableLKK2,026
- Implantable Pacemaker Pulse-GeneratorDXY956
- Permanent Pacemaker ElectrodeDTB358
- Implantable Cardioverter Defibrillator (Non-Crt)LWS191
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP182
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN157
- Pulse Generator, Permanent, ImplantableNVZ82
- Drug Eluting Permanent Left Ventricular (Lv) Pacemaker ElectrodeOJX75
- Programmer, PacemakerKRG51
- Mesh, Surgical, PolymericFTL43
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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