FDA Adverse Event
Injury
Summary report: N
APEX ARC HIP STEM
MDR report key: 4397888
·
Received January 4, 2015
Report
- Report Number
- MW5040040
- Event Type
- Injury
- Date Received
- January 4, 2015
- Date of Event
- February 20, 2012
- Report Date
- January 4, 2014
- Manufacturer
- OMNI LIFE SCIENCE
- Product Code
- LZO
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- FL, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Description of Event or Problem · 1
PATIENT HAD A LEFT TOTAL HIP ARTHROPLASTY ON (B)(6) 2012 FOR ADVANCED OSTEOARTHRITIS. THERE WERE NO COMPLICATIONS WITH THE SURGERY AND THE PT DID WELL FOR ELEVEN MONTHS. SHE COMPLAINED OF SWELLING OF THE WHOLE LEFT LOWER EXTREMITY AND A MASS MEDIALLY. AFTER MANY TESTS, A PSEUDOTUMOR CONSISTING OF NECROTIC TISSUE WAS FOUND. SHE UNDERWENT A LAPAROSCOPIC RESECTION OF THE LEFT RETROPERITONEAL TUMOR AND A REVISION LEFT TOTAL HIP ARTHROPLASTY WITH DEBUNKING OF THE PSEUDOTUMOR SEVEN DAYS LATER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1627 | APEX ARC HIP STEM | HIP PROSTHESIS, UNCEMENTED | LZO | OMNI LIFE SCIENCE | HC-21003-HA | 8629 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 68 YR | Hospitalization| R |