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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: INVACARE TAYLOR STREET ALL-IN-ONE-ALUMINUM COMMODE 4 PER CARTON 9153637754; ADAPTOR, HYGIENE

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INVACARE TAYLOR STREET ALL-IN-ONE-ALUMINUM COMMODE 4 PER CARTON 9153637754; ADAPTOR, HYGIENE Back to Search Results
Model Number 9650-4
Device Problems Collapse (1099); Component Falling (1105)
Patient Problem Fall (1848)
Event Date 05/23/2010
Event Type  malfunction  
Manufacturer Narrative
Mdr is being submitted as a result of a retrospective complaint review.Product was returned for an evaluation.This complaint appears to be a malfunction due to the distance between the laterals on the commode not being made to specifications.
 
Event Description
The consumer was using the commode when the left leg allegedly collapsed, causing her to fall backwards.
 
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Brand Name
ALL-IN-ONE-ALUMINUM COMMODE 4 PER CARTON 9153637754
Type of Device
ADAPTOR, HYGIENE
Manufacturer (Section D)
INVACARE TAYLOR STREET
1200 taylor street
elyria OH 44036
Manufacturer (Section G)
INVACARE TAYLOR STREET
1200 taylor street
elyria OH 44036
Manufacturer Contact
kevin guyton
one invacare way
elyria, OH 44035
8003336900
MDR Report Key5688320
MDR Text Key46187415
Report Number1525712-2016-01790
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 consumer
Reporter Occupation Patient Family Member or Friend
Type of Report Initial
Report Date 05/24/2010
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received05/31/2016
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model Number9650-4
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer06/08/2010
Is the Reporter a Health Professional? No
Date Manufacturer Received05/24/2010
Was Device Evaluated by Manufacturer? Yes
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 Age99
Patient Weight59
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