FDA Adverse Event
Injury
Summary report: N
UNKNOWN HIP
MDR report key: 6299052
·
Received February 2, 2017
Report
- Report Number
- 0001822565-2017-00443
- Event Type
- Injury
- Date Received
- February 2, 2017
- Report Date
- January 30, 2017
- Manufacturer
- ZIMMER, INC.
- Product Code
- JDI
- PMA / PMN Number
- PNI
- Removal / Correction Number
- N/A
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FR
- Reporter Occupation
- PHYSICIAN
Narratives
Additional Manufacturer Narrative · 1
CURRENT INFORMATION IS INSUFFICIENT TO PERMIT A CONCLUSION AS TO THE CAUSE OF THE EVENT. THE PRODUCT IDENTIFICATION NECESSARY TO REVIEW MANUFACTURING HISTORY WAS NOT PROVIDED. MATTHIEU OLLIVIER, ET AL. ¿USE OF POROUS TANTALUM COMPONENTS IN PAPROSKY TWO AND THREE ACETABULAR REVISION. A MINIMUM FIVE-YEAR FOLLOW-UP OF FIFTY ONE HIPS.¿ 10.1007/S00264-016-3312-2.
Description of Event or Problem · 1
IT WAS REPORTED IN A JOURNAL ARTICLE THAT A PATIENT EXPERIENCED A FRACTURED SCREW IN ONE HIP AND A HARRIS HIP SCORE OF 78. NO REVISION PROCEDURE WAS REPORTED AND PATIENT OUTCOME IS UNKNOWN.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 78815 | UNKNOWN HIP | PROSTHESIS, HIP | JDI | ZIMMER, INC. | N/A | NI |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |