TOUCH N' HEAT 973-0212

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 08 report with the FDA on 2013-08-26 for TOUCH N' HEAT 973-0212 manufactured by Sybronendo.

Event Text Entries

[20982545] A doctor's office had alleged that two (2) touch n' heat units had continued heating up when not in use and plugged in. This is the second of two (2) reports.
Patient Sequence No: 1, Text Type: D, B5


[21142328] No further information was received with regard to this incident. Multiple attempts were made to contact the complainant in order to obtain further information; however, the complainant has remained unresponsive. An update will be provided if any new information becomes available. A visual and physical evaluation of the returned device revealed that a spring was bent on the device, causing constant heating.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2016150-2013-00101
MDR Report Key3307072
Report Source08
Date Received2013-08-26
Date of Report2013-07-26
Date Mfgr Received2013-07-26
Date Added to Maude2013-11-22
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactMRS. KERRI CASINO
Manufacturer Street1717 W. COLLINS AVE
Manufacturer CityORANGE CA 29867
Manufacturer CountryUS
Manufacturer Postal29867
Manufacturer Phone7145167634
Manufacturer G1SYBRONENDO
Manufacturer Street1332 SOUTH LONE HILL AVENUE
Manufacturer CityGLENDORA CA 91740
Manufacturer CountryUS
Manufacturer Postal Code91740
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTOUCH N' HEAT
Generic NamePULP TESTER
Product CodeEAT
Date Received2013-08-26
Catalog Number973-0212
OperatorOTHER
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSYBRONENDO
Manufacturer Address1332 SOUTH LONE HILL AVENUE GLENDORA CA 91740 US 91740


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2013-08-26

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