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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: EXACTECH, INC. EQUINOXE HUMERAL STEM, PRIMARY, PRESS-FIT

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EXACTECH, INC. EQUINOXE HUMERAL STEM, PRIMARY, PRESS-FIT Back to Search Results
Catalog Number 300-01-11
Device Problem Insufficient Information (3190)
Patient Problems Fall (1848); Complaint, Ill-Defined (2331)
Event Date 04/03/2012
Event Type  Injury  
Event Description
Patient presents with arm soreness after a fall, claims soreness is not related to fall.No reported revision of components was received.This event report was received through clinical data collection activities.
 
Manufacturer Narrative
The contribution of the devices to the experience reported could not be determined as the devices were not returned for evaluation.Additionally, the device specific identification information was not provided, precluding a review of the device history record.
 
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Brand Name
EQUINOXE HUMERAL STEM, PRIMARY, PRESS-FIT
Type of Device
HUMERAL STEM, PRIMARY
Manufacturer (Section D)
EXACTECH, INC.
2320 n.w. 66th ct.
gainesville FL 32653
Manufacturer Contact
graham cuthbert
2320 n.w. 66th ct.
gainesville, FL 32653
MDR Report Key3863029
MDR Text Key4511731
Report Number1038671-2014-00204
Device Sequence Number1
Product Code KWT
Combination Product (y/n)N
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Company Representative
Reporter Occupation Other
Type of Report Initial
Report Date 06/05/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Catalogue Number300-01-11
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Initial Date Manufacturer Received 05/15/2014
Initial Date FDA Received06/06/2014
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Patient Outcome(s) Other;
Patient Age59 YR
Patient Weight73
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