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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: JUNCHENG CANE, CRUTCH AND WALKER TIPS AND PADS; 890.3790

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JUNCHENG CANE, CRUTCH AND WALKER TIPS AND PADS; 890.3790 Back to Search Results
Model Number 6271
Device Problem Product Quality Problem (1506)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Type  No Answer Provided  
Event Description
It was reported that the fixed wheel attachments on the walker have a faulty spring.
 
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Brand Name
CANE, CRUTCH AND WALKER TIPS AND PADS
Type of Device
890.3790
Manufacturer (Section D)
JUNCHENG
zhongshan
CH 
MDR Report Key3562057
MDR Text Key4076888
Report Number1531186-2014-00101
Device Sequence Number1
Product Code INP
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 01/08/2014,12/27/2013
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received01/08/2014
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model Number6271
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Was the Report Sent to FDA? Yes
Date Report Sent to FDA01/08/2014
Distributor Facility Aware Date12/27/2013
Date Report to Manufacturer01/08/2014
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Other;
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