HTR5500 HTR-DELUXE MODEL 5500 9153635378

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-11-06 for HTR5500 HTR-DELUXE MODEL 5500 9153635378 manufactured by Invacare Taylor Street.

Event Text Entries

[30879381] Should additional information become available for the patient a supplemental record will be filed.
Patient Sequence No: 1, Text Type: N, H10


[30879382] The right front caster is broken, seems bent.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1525712-2015-05268
MDR Report Key5207053
Date Received2015-11-06
Date of Report2015-10-16
Date Mfgr Received2015-10-16
Date Added to Maude2015-11-06
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPATIENT FAMILY MEMBER OR FRIEND
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactKEVIN GUYTON
Manufacturer StreetONE INVACARE WAY
Manufacturer CityELYRIA OH 44035
Manufacturer CountryUS
Manufacturer Postal44035
Manufacturer Phone8003336900
Manufacturer G1INVACARE TAYLOR STREET
Manufacturer Street1200 TAYLOR STREET
Manufacturer CityELYRIA OH 44036
Manufacturer CountryUS
Manufacturer Postal Code44036
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameHTR5500 HTR-DELUXE MODEL 5500 9153635378
Generic NameCHAIR AND TABLE, MEDICAL
Product CodeKMN
Date Received2015-11-06
Model NumberHTR5500
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerINVACARE TAYLOR STREET
Manufacturer Address1200 TAYLOR STREET ELYRIA OH 44036 US 44036


Patients

Patient NumberTreatmentOutcomeDate
10 2015-11-06

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