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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: DEPUY TRI-LOCK BPS W/GRIPTION FEMORAL STEM STD OFFSETNONE

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DEPUY TRI-LOCK BPS W/GRIPTION FEMORAL STEM STD OFFSET NONE   Back to Search Results
Catalog Number 1012-04-080
Event Date 02/16/2009
Event Type  Injury   Patient Outcome  Disability
Event Description

I had a left hip replacement (depuy pinnacle) on (b)(6) 2009 and ever since (b)(6) 2010 i have had a problem which keeps getting worse. I have difficulty standing still for any length of time. If i stand for 10 minutes shaving, i am in severe pain for the rest of the day. I can only sleep on my right side. I cannot sleep on my back or left side at all because the pain is too much. I cannot food shop, clothes shop or shop period because i cannot walk for any length of time. Unless my activity includes sitting such as the movies, out to dinner or the doctor's office, i cannot go out. The quality of my life has deteriorated. I am in worse shape now then i was before i got my hip replaced. When i saw the doctor who replaced my hip regarding my pain i was in he took an x-ray said everything was ok and don't bother wasting your co-pay coming back. Nice!!! so now i have gone for a second opinion. However, because this hip has not been recalled it seems no one really wants to make the tough decisions associated with a hip replacement gone bad. I would like some relief which i do not seem to be able to get. Help! help! help me please! give me my life back! the only common denominator is a hip replacement. I had a left hip replacement and now i cannot walk on my left leg for any period of time. What else could it be? please everyone use your common sense. On a scale of one to ten, my pain is usually a seven.

 
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Brand NameDEPUY TRI-LOCK BPS W/GRIPTION FEMORAL STEM STD OFFSET
Type of DeviceNONE
Device Event Key1969493
MDR Report Key1937943
Event Key1834939
Report NumberMW5018672
Device Sequence Number4
Product CodeKWY
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 12/20/2010
5 DeviceS WERE Involved in the Event:1 2 3 4 5 
1 Patient Was Involved in the Event
Date FDA Received12/20/2010
Is This An Adverse Event Report? No
Is This A Product Problem Report? Yes
Device Operator Lay User/Patient
Device Catalogue Number1012-04-080
Device LOT NumberCB1HJ1000
Is The Reporter A Health Professional? No
Was The Report Sent To Manufacturer? No
Is the Device an Implant? Yes
Is this an Explanted Device?

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