FEMORAL HEAD
Report
- Report Number
- 0002648920-2018-00047
- Event Type
- Injury
- Date Received
- January 17, 2018
- Report Date
- March 23, 2018
- Manufacturer
- ZIMMER MANUFACTURING B.V.
- Product Code
- LPH
- PMA / PMN Number
- PK953337
- Removal / Correction Number
- N/A
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- PATIENT
Narratives
(B)(4) MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT. PLEASE SEE REPORTS: 0001822565-2018-00392, 0001822565-2018-00393, 0001822565-2018-00394, 0001822565-2018-00395. CONCOMITANT MEDICAL PRODUCTS: 00784800200 MODULAR NECK K 12/14 NECK TAPER USE WITH +0 HEADS ONLY LOT 61218348, 00771301300 MODULAR FEMORAL STEM PRESS-FIT PLASMA SPRAYED CEMENTLESS SIZE 13.5 LOT 61375744, 65620005422 SHELL POROUS WITH CLUSTER HOLES 54 MM O.D. WITH CALCICOAT CERAMIC COATING LOT 61330651, 00631005032 LINER 10 DEGREE ELEVATED RIM 32 MM I.D. FOR USE WITH 50/52/54 MM O.D. SHELLS LOT 61365043. THE INVESTIGATION IS IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED. DEVICE REMAINS IMPLANTED.
UPON REASSESSMENT OF THE REPORTED EVENT IT WAS DETERMINED THAT THIS EVENT WILL BE REPORTED ON MFR NUMBER 1822565-2011-02059-1.
IT WAS REPORTED THAT A PATIENT UNDERWENT A LEFT INITIAL TOTAL HIP ARTHROPLASTY DUE TO DEGENERATIVE ARTHRITIS. SUBSEQUENTLY, THE PATIENT IS EXPERIENCING SEVERE PAIN IN THE GROIN AND TIBIAL AREA. THE PATIENT HAS BEEN DOING ONGOING TREATMENT FOR THIS PAIN WITH MULTIPLE PROCEDURES AND IS REFUSING A REVISION PROCEDURE. NO FURTHER INFORMATION IS AVAILABLE AT THIS TIME.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 46282 | FEMORAL HEAD | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED | LPH | ZIMMER MANUFACTURING B.V. | N/A | 61426909 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |