TESS HUMERAL REVERSE COROLLA S0
Report
- Report Number
- 3006946279-2016-00434
- Event Type
- Injury
- Date Received
- November 18, 2016
- Date of Event
- October 19, 2016
- Report Date
- April 28, 2017
- Manufacturer
- BIOMET FRANCE S.A.R.L.
- Product Code
- KWS
- PMA / PMN Number
- PK060694
- Removal / Correction Number
- N/A
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FR
- Reporter Occupation
- PHYSICIAN
Narratives
UPON REASSESSMENT OF THE REPORTED EVENT, IT WAS DETERMINED TO BE NOT REPORTABLE. THE INITIAL REPORT WAS FORWARDED IN ERROR AND SHOULD BE VOIDED.
THE PRODUCT IDENTIFICATION NECESSARY TO REVIEW MANUFACTURING HISTORY WAS NOT PROVIDED. CURRENT INFORMATION IS INSUFFICIENT TO PERMIT A CONCLUSION AS TO THE CAUSE OF THE EVENT. (B)(4). THIS USER FACILITY IS OUTSIDE OF THE UNITED STATES. CURRENT INFORMATION IS INSUFFICIENT TO PERMIT A CONCLUSION AS TO THE CAUSE OF THE EVENT. THIS PRODUCT IS MANUFACTURED BY ZIMMER BIOMET (B)(4) AND IS NOT CLEARED OR DISTRIBUTED IN THE U.S. HOWEVER, THIS REPORT IS BEING SUBMITTED AS ZIMMER BIOMET IN (B)(6) MANUFACTURES A SIMILAR DEVICE IN THE UNITED STATES UNDER 510K NUMBER K060694. THIS REPORT IS NUMBER 1 OF 2 MDRS FILED FOR THE SAME PATIENT (REFERENCE 3006946279-2016-00434 / 00435).
DURING A SHOULDER ARTHROPLASTY, THE HUMERAL INLAY AND COROLLA DID NOT ASSEMBLE AS EXPECTED, AND AS A RESULT THE COROLLA AND HUMERAL INLAY WERE REMOVED AND REPLACED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 765072 | TESS HUMERAL REVERSE COROLLA S0 | PROSTHESIS, SHOULDER | KWS | BIOMET FRANCE S.A.R.L. | N/A | 0001098407 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 75 YR | Required Intervention |