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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: CONSMA MECHANICAL WALKER, ROLLATOR; 890.3825

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CONSMA MECHANICAL WALKER, ROLLATOR; 890.3825 Back to Search Results
Model Number 65851B
Device Problems Break (1069); Crack (1135)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Date 09/24/2014
Event Type  No Answer Provided  
Event Description
End user advised seat cracked and broke in half.
 
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Brand Name
MECHANICAL WALKER, ROLLATOR
Type of Device
890.3825
Manufacturer (Section D)
CONSMA
no. 158 huicheng rd
huimin ind
jianshan zhejiang 3141 12
CH  314112
MDR Report Key4211297
MDR Text Key4966392
Report Number1531186-2014-05185
Device Sequence Number1
Product Code ITJ
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 Patient
Type of Report Initial
Report Date 10/29/2014,10/08/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model Number65851B
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Was the Report Sent to FDA? Yes
Date Report Sent to FDA10/29/2014
Distributor Facility Aware Date10/08/2014
Device Age22 MO
Date Report to Manufacturer10/29/2014
Initial Date Manufacturer Received Not provided
Initial Date FDA Received10/29/2014
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Other;
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