Valleylab
FDA adverse event reports naming Valleylab as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: VALLEYLAB.
- Total reports
- 1,794
- Deaths
- 30
- Injuries
- 541
- Malfunctions
- 1,123
Reports per year
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
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI1,621
- Electrode, ElectrosurgicalJOS114
- Device, Hemostasis, VascularMGB12
- Unit, ElectrosurgicalFAR6
- Unit, Electrosurgical, Endoscopic (With Or Without Accessories)KNS6
- Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, ReprocessedNUJ5
- Electrosurgical Patient Return ElectrodeODR5
- Neurosurgical Ultrasonic InstrumentsLBK4
- Laparoscope, General & Plastic SurgeryGCJ3
- Generator, Lesion, RadiofrequencyGXD3
Recent recalls
- 2003-08-12TerminatedOther
Radionics Disposable Grounding Plate
Pads may have a thin plastic film covering the conductive gel surface underneath the normal printed cover, causing non-adherence and possible burn.
- 2003-08-12TerminatedOther
Radionics Cool-Tip RF Electrode Kit, containing DGP-HP single-use grounding pads.
Pads may have a thin plastic film covering the conductive gel surface underneath the normal printed cover, causing non-adherence and possible burn.
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