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 2011-11-22 for DAILY ACTIVITY ASSIST DEVICES 9630-4 manufactured by Invamex.

Event Text Entries

[2355338] The seat on the commode is allegedly cracked. No injury is alleged.
Patient Sequence No: 1, Text Type: D, B5


[9469638] No rma has been initiated for this issue. Model 9630-4, serial number/date code is unknown. The user manual part number 1148075 was issued with this device. The user manual is also found on-line at invacare. Com. It is unknown if the consumer has fully read and understands the user manual. Documentation provides warnings, cautions, and instructions for safely using the device. If the consumer does not understand the written warnings, cautions or instructions then they should contact invacare. The consumers medical condition, stability and medication regimen are unknown. The consumers age, height and weight are unknown. The consumers technique while using the device is unknown. The maintenance history of the device is unknown.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number9616091-2011-00120
MDR Report Key2344910
Report Source08
Date Received2011-11-22
Date of Report2011-11-21
Date Mfgr Received2011-10-28
Date Added to Maude2012-07-18
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 FDA0
Event Location0
Manufacturer ContactKAREN LOUGHREN
Manufacturer StreetONE INVACARE WAY
Manufacturer CityELYRIA OH 44036
Manufacturer CountryUS
Manufacturer Postal44036
Manufacturer Phone8003336900
Manufacturer G1INVAMEX
Manufacturer StreetP O DRAWER BB
Manufacturer CityHIDALGO TX 78557
Manufacturer CountryUS
Manufacturer Postal Code78557
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDAILY ACTIVITY ASSIST DEVICES
Generic Name890.5050
Product CodeILZ
Date Received2011-11-22
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 2011-11-22

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