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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: INVAMEX DROP ARM COMMODE 9153630715; ADAPTOR, HYGIENE

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INVAMEX DROP ARM COMMODE 9153630715; ADAPTOR, HYGIENE Back to Search Results
Model Number 9669
Device Problems Sticking (1597); Device Inoperable (1663)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Type  malfunction  
Event Description
Dealer states the left rear extension leg is stuck, the snap button is not visible and leg cannot be removed.
 
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Brand Name
DROP ARM COMMODE 9153630715
Type of Device
ADAPTOR, HYGIENE
Manufacturer (Section D)
INVAMEX
parque industrial manimex
reynosa 8878 0
MX  88780
Manufacturer (Section G)
INVAMEX
parque industrial manimex
reynosa 8878 0
MX   88780
Manufacturer Contact
kevin guyton
one invacare way
elyria, OH 44036
8003336900
MDR Report Key4410192
MDR Text Key5283488
Report Number9616091-2015-00101
Device Sequence Number1
Product Code ILS
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Distributor
Reporter Occupation Medical Equipment Company Technician/Representative
Type of Report Initial
Report Date 12/26/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received01/12/2015
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model Number9669
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received12/26/2014
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse
Patient Sequence Number1
Patient Outcome(s) Other;
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