• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: TOM PALADINO AND SCALARLIGHT / SCALAR LIGHT SCALAR ENGERY LAMP, INFRARED, THERAPEUTIC HEATING

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

TOM PALADINO AND SCALARLIGHT / SCALAR LIGHT SCALAR ENGERY LAMP, INFRARED, THERAPEUTIC HEATING Back to Search Results
Device Problem Adverse Event Without Identified Device or Use Problem (2993)
Patient Problem Insufficient Information (4580)
Event Type  Injury  
Event Description
(b)(6) and scalar light are lying to people, pushing an imaginary "health solution" - they are making over (b)(4) a month from people promising the cure cancer, addiction, weight problems and more and it's all fake. People are dying because they stop working with their doctors to get his fake science from god's hand. Fda safety report id # (b)(4).
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand NameSCALAR ENGERY
Type of DeviceLAMP, INFRARED, THERAPEUTIC HEATING
Manufacturer (Section D)
TOM PALADINO AND SCALARLIGHT / SCALAR LIGHT
po box 1628
santa maria CA 93456
MDR Report Key12238955
MDR Text Key264090208
Report NumberMW5102803
Device Sequence Number1
Product Code ILY
Combination Product (y/n)Y
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Type of Report Initial
Report Date 07/24/2021
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received07/27/2021
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Operator
Was Device Available for Evaluation? No
Was the Report Sent to FDA?
Event Location No Information
Was Device Evaluated by Manufacturer?
Is the Device Single Use?
Is This a Reprocessed and Reused Single-Use Device?
Type of Device Usage

Patient Treatment Data
Date Received: 07/27/2021 Patient Sequence Number: 1
-
-