TPS CORD 5100004000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2019-04-26 for TPS CORD 5100004000 manufactured by Stryker Instruments-kalamazoo.

Event Text Entries

[143308485] The user facility reported that the device overheated during the procedure and the patient received a 2cm burn with blister on the lip. The burn was treated with silvadene. There were no other adverse consequences regarding the event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001811755-2019-01539
MDR Report Key8557302
Report SourceUSER FACILITY
Date Received2019-04-26
Date of Report2019-06-14
Date of Event2019-04-03
Date Mfgr Received2019-06-14
Device Manufacturer Date2017-10-27
Date Added to Maude2019-04-26
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 FDA3
Event Location3
Manufacturer ContactMR. ZACH BAKER
Manufacturer Street4100 EAST MILHAM AVENUE
Manufacturer CityKALAMAZOO MI 49001
Manufacturer CountryUS
Manufacturer Postal49001
Manufacturer Phone2693237700
Manufacturer G1STRYKER INSTRUMENTS-KALAMAZOO
Manufacturer Street4100 EAST MILHAM AVENUE
Manufacturer CityKALAMAZOO MI 49001
Manufacturer CountryUS
Manufacturer Postal Code49001
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTPS CORD
Generic NameDENTAL OPERATIVE UNIT AND ACCESSORIES.
Product CodeEIA
Date Received2019-04-26
Catalog Number5100004000
Lot Number17300
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER INSTRUMENTS-KALAMAZOO
Manufacturer Address4100 EAST MILHAM AVENUE KALAMAZOO MI 49001 US 49001


Patients

Patient NumberTreatmentOutcomeDate
10 2019-04-26

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.