GUARDIAN EASY CARE WALKER 30756P

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-08-02 for GUARDIAN EASY CARE WALKER 30756P manufactured by Sunrise Medical (us) Llc.

MAUDE Entry Details

Report Number2937137-2019-00021
MDR Report Key8857860
Date Received2019-08-02
Date of Report2019-07-05
Date of Event2018-04-23
Date Mfgr Received2019-07-05
Device Manufacturer Date2004-12-09
Date Added to Maude2019-08-02
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. GUSTAVO ZAMBRANO
Manufacturer Street2842 BUSINESS PARK AVE.
Manufacturer CityFRESNO CA 93727
Manufacturer CountryUS
Manufacturer Postal93727
Manufacturer Phone5592942840
Manufacturer G1SUNRISE MEDICAL (US) LLC
Manufacturer Street2842 BUSINESS PARK AVE.
Manufacturer CityFRESNO CA 93727
Manufacturer CountryUS
Manufacturer Postal Code93727
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameGUARDIAN EASY CARE WALKER
Generic NameWALKER
Product CodeNXE
Date Received2019-08-02
Model Number30756P
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSUNRISE MEDICAL (US) LLC
Manufacturer Address2842 BUSINESS PARK AVE. FRESNO CA 93727 US 93727


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization 2019-08-02

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