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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: GUIDE WIRE; ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
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GUIDE WIRE; ORTHOPEDIC MANUAL SURGICAL INSTRUMENT Back to Search Results
Device Problem Material Twisted/Bent (2981)
Patient Problem Insufficient Information (4580)
Event Description
Guidewire bent while reaming phalangeal side of 1st mtp joint.Fda safety report id# (b)(4).
 
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Brand Name
GUIDE WIRE
Type of Device
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
MDR Report Key14015077
MDR Text Key288799700
Report NumberMW5108762
Device Sequence Number2
Product Code LZJ
Combination Product (y/n)N
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Other
Type of Report Initial
Report Date 04/01/2022
2 Devices were Involved in the Event: 1   2  
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? No
Initial Date Manufacturer Received Not provided
Initial Date FDA Received04/04/2022
Patient Sequence Number1
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