UNKNOWN EXTREMITY
Report
- Report Number
- 3006946279-2016-00096
- Event Type
- Injury
- Date Received
- May 27, 2016
- Report Date
- April 28, 2016
- Manufacturer
- BIOMET FRANCE S.A.R.L.
- Product Code
- MJT
- PMA / PMN Number
- PNI
- Removal / Correction Number
- N/A
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- SW
- Reporter Occupation
- PHYSICIAN
Narratives
CURRENT INFORMATION IS INSUFFICIENT TO PERMIT CONCLUSIONS AS TO THE CAUSE OF THE EVENTS. EVENT DETAILS AND PRODUCT IDENTIFICATION WERE NOT PROVIDED FOR THE PATIENTS MENTIONED IN THE JOURNAL ARTICLE. THIS IS NUMBER 2 OF 2 MDRS FILED FOR THE SAME EVENTS (REFERENCE 1825034-2016-01732 AND 3006946279-2016-00096).
INFORMATION WAS RECEIVED BASED ON A REVIEW OF THE JOURNAL ARTICLE, "ASSOCIATION OF LATERAL HUMERAL OFFSET WITH FUNCTIONAL OUTCOME AND GEOMETRIC RESTORATION IN STEMLESS TOTAL SHOULDER ARTHROPLASTY." THE AIMS OF THIS STUDY WERE TO DETERMINE THE ASSOCIATION OF POSTOPERATIVE LATERAL HUMERAL OFFSET (LHO) CHANGES WITH SHOULDER FUNCTION AND QUALITY OF LIFE AND TO INVESTIGATE THE ABILITY OF STEMLESS ANATOMIC TOTAL SHOULDER ARTHROPLASTY TO RESTORE LHO, HUMERAL HEAD HEIGHT (HH), CENTER OF ROTATION (COR), AND NECK-SHAFT ANGLE (NSA). THE HYPOTHESIS WAS THAT POSTOPERATIVE LHO CHANGES WOULD INFLUENCE SHOULDER FUNCTION AND QUALITY OF LIFE AND THE STEMLESS ANATOMIC TOTAL SHOULDER ARTHROPLASTY (TSA) WOULD RESTORE THE TESTED GEOMETRIC PARAMETERS TO ACCEPTABLE LIMITS. TWO PATIENTS IDENTIFIED IN THE ARTICLE WERE REPORTED TO HAVE EXPERIENCED POST-TRAUMATIC OSTEOARTHRITIS FOLLOWING IMPLANTATION OF THE DEVICE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 341444 | UNKNOWN EXTREMITY | PROSTHESIS, SHOULDER | MJT | BIOMET FRANCE S.A.R.L. | N/A | NI |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |