DAILY ACTIVITY ASSIST DEVICES 9630-4

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 2012-07-16 for DAILY ACTIVITY ASSIST DEVICES 9630-4 manufactured by Invamex.

Event Text Entries

[2772284] "per consumer, alleges noticed a few months ago (2-3) that there is a crack in the seat of the commode. "
Patient Sequence No: 1, Text Type: D, B5


[10096779] No rma has been initiated for this event. Model 9630-4, serial number/date code is unknown. The owner's manual was issued with this device. The owner's manual is also found on-line at invacare. Com. It is unknown if the consumer has fully read and understands the owner's manual. Documentation provides warnings, cautions, and instructions for safely using the device. The consumer's age, height and weight are unknown. The consumer's medical condition, stability and medication regimen are unknown. The consumer's technique while using the device is unknown. The maintenance history of the device is unknown. The consumer alleges that there is a crack in the seat of the commode.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number9616091-2012-00208
MDR Report Key2655973
Report Source08
Date Received2012-07-16
Date of Report2012-07-14
Date Mfgr Received2012-06-21
Date Added to Maude2012-11-01
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
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactNATALIE WILLIAMS
Manufacturer StreetONE INVACARE WAY
Manufacturer CityELYRIA OH 44035
Manufacturer CountryUS
Manufacturer Postal44035
Manufacturer Phone8003336900
Manufacturer G1INVAMEX
Manufacturer StreetP O DRAWER BB
Manufacturer CityHIDALGO TX 78557
Manufacturer CountryUS
Manufacturer Postal Code78557
Single Use0
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDAILY ACTIVITY ASSIST DEVICES
Generic Name890.5050
Product CodeINB
Date Received2012-07-16
Model Number9630-4
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerINVAMEX
Manufacturer AddressP O DRAWER BB HIDALGO TX 78557 US 78557


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2012-07-16

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