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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US GLOBAL ADVANTAGE STEM 8 MM; GLOBAL ADVANTAGE IMPLANT : SHOULDER HUMERAL STEMS

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DEPUY ORTHOPAEDICS INC US GLOBAL ADVANTAGE STEM 8 MM; GLOBAL ADVANTAGE IMPLANT : SHOULDER HUMERAL STEMS Back to Search Results
Model Number 1137-08-000
Device Problem Adverse Event Without Identified Device or Use Problem (2993)
Patient Problems Pain (1994); Limited Mobility Of The Implanted Joint (2671); No Code Available (3191)
Event Date 12/04/2019
Event Type  Injury  
Manufacturer Narrative
(b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
 
Event Description
Patient presented in clinic with painful right shoulder surgeon had replaced in (b)(6) 2003 at (b)(6).Patient also exhibited loss of function in right shoulder so the doctor elected to perform a revision surgery on patient¿s right shoulder.Performed revision surgery on (b)(6) 2019 at (b)(6).Surgeon removed the glenoid, humeral stem, and humeral head with instrumentation.He then elected to implant a reverse shoulder prosthesis using competitive systems.
 
Manufacturer Narrative
Depuy synthes is submitting this report pursuant to the provision of 21 cfr, part 803.The report may be based on the information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.H10 additional narrative: corrected: h6.Product complaint # (b)(4).Investigation summary - the device associated with this report was not received for examination.Depuy synthes considers the investigation closed at this time.Should additional information be received, the information will be reviewed and the investigation may be re-opened as necessary.Device history lot - null.Device history batch - null.Device history review - null.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
 
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Brand Name
GLOBAL ADVANTAGE STEM 8 MM
Type of Device
GLOBAL ADVANTAGE IMPLANT : SHOULDER HUMERAL STEMS
Manufacturer (Section D)
DEPUY ORTHOPAEDICS INC US
700 orthopaedic drive
warsaw IN 46581 0988
MDR Report Key9519695
MDR Text Key174708782
Report Number1818910-2019-124627
Device Sequence Number1
Product Code HSD
UDI-Device Identifier10603295007081
UDI-Public10603295007081
Combination Product (y/n)N
PMA/PMN Number
K992065
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative,health
Type of Report Initial,Followup
Report Date 12/04/2019
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received12/26/2019
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Model Number1137-08-000
Device Catalogue Number113708000
Was Device Available for Evaluation? No
Date Manufacturer Received01/22/2020
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Required Intervention;
Patient Age84 YR
Patient Weight59
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