3 POSITION RECLINER DELUXE-X WIDE ROSEWOOD 9153641330 6980-93

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-11-03 for 3 POSITION RECLINER DELUXE-X WIDE ROSEWOOD 9153641330 6980-93 manufactured by Unknown.

Event Text Entries

[30497049] Should additional information become available for the patient a supplemental record will be filed.
Patient Sequence No: 1, Text Type: N, H10


[30497050] The dealer called stating that the lift out chair model pendant is not working all the time. He alleges it's working intermittently if you jiggle the cable.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1525712-2015-05187
MDR Report Key5197038
Date Received2015-11-03
Date of Report2015-10-06
Date Mfgr Received2015-10-06
Date Added to Maude2015-11-03
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationMEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE
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 G1UNKNOWN
Manufacturer CityOH
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand Name3 POSITION RECLINER DELUXE-X WIDE ROSEWOOD 9153641330
Generic NameCHAIR AND TABLE, MEDICAL
Product CodeKMN
Date Received2015-11-03
Model Number6980-93
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerUNKNOWN
Manufacturer AddressOH US


Patients

Patient NumberTreatmentOutcomeDate
10 2015-11-03

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