UNKNOWN DEPUY AML STEM
Report
- Report Number
- 1818910-2013-06546
- Event Type
- Malfunction
- Date Received
- May 31, 2013
- Date of Event
- November 7, 2012
- Report Date
- May 8, 2013
- Manufacturer
- DEPUY WARSAW
- Product Code
- JDI
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- PHYSICIAN
Narratives
MEDICAL RECORDS WERE PROVIDED AND REVIEWED. THE INVESTIGATION COULD NOT DRAW ANY CONCLUSIONS REGARDING THE REPORTED EVENT WITH THE INFORMATION AVAILABLE. BASED ON THE INABILITY TO IDENTIFY A ROOT CAUSE, THE NEED FOR CORRECTIVE ACTION WAS NOT INDICATED. DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD ANY ADDITIONAL INFORMATION BE RECEIVED TO CHANGE THE OUTCOME OF THE PERFORMED INVESTIGATION, THE COMPLAINT WILL BE RE-OPENED.
THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED.
THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED.
PATIENT WAS REVISED TO ADDRESS ONGOING INFECTION. UPDATE (B)(4) 2013 - PATIENT'S MEDICAL RECORDS WERE RECEIVED. RECORDS INDICATE THE PATIENT WAS REVISED ON (B)(6) 2012 TO ADDRESS BURSITIS AND WOUND DRAINAGE. UPON REVISION FRETTING AND CORROSION WAS NOTED ON TRUNNION OF THE FEMORAL COMPONENT. THE METAL INSERT WAS REMOVED. THE PATIENT WAS REIMPLANTED ON (B)(6) 2012, AT WHICH TIME THE FEMORAL HEAD WAS REMOVED. RECORDS INDICATE THERE WAS OSTEOLYSIS NOTED IN THE HIP ALONG WITH GRAYISH GRUMOUS/CASEATING TYPE MATERIAL.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 241650 | UNKNOWN DEPUY AML STEM | STEM | JDI | DEPUY WARSAW | NI |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 61 YR |