Lake Region Medical
FDA adverse event reports naming Lake Region Medical as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: LAKE REGION MEDICAL.
- Total reports
- 1,519
- Deaths
- 92
- Injuries
- 411
- Malfunctions
- 1,015
Reports per year
412
413
1514
9715
10816
13617
10018
11119
10420
10021
12722
19823
20024
13325
7526
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Wire, Guide, CatheterDQX1,257
- Stylet, UreteralEYA126
- Stylet For Catheter, Gastro-UrologyEZB96
- Hysteroscope (And Accessories)HIH13
- Endoscopic Guidewire, Gastroenterology-UrologyOCY13
- Forceps, Biopsy, Non-ElectricFCL3
- Forceps, General & Plastic SurgeryGEN3
- Tester, Electrode/Lead, ElectroencephalographGYA3
- Catheter, Electrode Recording, Or Probe, Electrode RecordingDRF1
- Laparoscope, General & Plastic SurgeryGCJ1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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