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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: GOODBABY MECHANICAL (MANUAL) WHEELCHAIR; 890.3850

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GOODBABY MECHANICAL (MANUAL) WHEELCHAIR; 890.3850 Back to Search Results
Model Number TREX28R
Device Problem Material Separation (1562)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Type  No Answer Provided  
Event Description
Per provider the wheels are rolling off of the rim.
 
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Brand Name
MECHANICAL (MANUAL) WHEELCHAIR
Type of Device
890.3850
Manufacturer (Section D)
GOODBABY
CH 
MDR Report Key4180021
MDR Text Key5097980
Report Number1531186-2014-04925
Device Sequence Number1
Product Code IOR
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Invalid Data
Reporter Occupation Medical Equipment Company Technician/Representative
Type of Report Initial
Report Date 10/16/2014,09/26/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received10/17/2014
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model NumberTREX28R
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Was the Report Sent to FDA? Yes
Date Report Sent to FDA10/16/2014
Distributor Facility Aware Date09/26/2014
Date Report to Manufacturer10/16/2014
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Other;
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