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Recall

Class II — Med-Hot Thermal Imaging, Inc.

Recalling firmMED-HOT THERMAL IMAGING, INC
Registered facilityMED-HOT THERMAL IMAGING, INC (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonIndications for use are not cleared or approved for market in the U.S.
ProductMEDHOT MTI 2000 THERMAL IMAGING SYSTEM - TotalVision software with Elevated Body Temperature Screening module, for use as a medical diagnostic purposes as part of a telethermographic system utilizing FLIR cameras, Models A615sc and A315sc. Cameras are private labeled as MAX Basic, MAX 76 and MAX 307.
Quantity12
DistributionUS: AL and NJ - Foreign: Nigeria
Initiated2017-01-14
Classified2017-05-09
Terminated2019-08-07
Recall numberZ-2057-2017
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Med-Hot Thermal Imaging, Inc. (Z-2057-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/76622/

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