COMPR SRS 50MM DST HUM BDY RT
Report
- Report Number
- 0001825034-2018-11334
- Event Type
- Injury
- Date Received
- January 7, 2019
- Date of Event
- October 12, 2018
- Report Date
- January 23, 2019
- Manufacturer
- ZIMMER BIOMET, INC.
- Product Code
- JDC
- PMA / PMN Number
- K153398
- Removal / Correction Number
- N/A
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA
- Reporter Occupation
- PHYSICIAN
Narratives
UPON REASSESSMENT OF THE REPORTED EVENT BASED ON THE ADDITIONAL INFORMATION, IT WAS DETERMINED THAT THE PRODUCT IS NOT REPORTABLE. THE EVENT IS NOT PROCEDURE OR IMPLANT RELATED.
(B)(4). CONCOMITANT MEDICAL PRODUCTS: 211225 COMPR SRS IC SEG - 60MM 875550, 211238 COMPR SRS MOD STEM - 12X100MM 653050, UNKNOWN NEXEL ULNAR COMPONENT, UNKNOWN NEXEL ULNAR ARTICLUATION COMPONENT. (B)(6). THE COMPLAINT IS UNDER INVESTIGATION. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034 - 2018 - 11332, 0001825034 - 2018 - 11333.
NO ADDITIONAL INFORMATION IS AVAILABLE TO REPORT AT THIS TIME.
IT WAS REPORTED THAT PATIENT UNDERWENT AN INITIAL RIGHT DISTAL HUMERAL RESECTION WITH RECONSTRUCTION INVOLVING AN ELBOW ARTHROPLASTY, AND RECEIVED BLOOD TRANSFUSION DUE TO POSTOPERATIVE ANEMIA. IT WAS MENTIONED THAT THE EVENT IS PROCEDURE RELATED AND NOT DEVICE RELATED. NO OTHER ADDITIONAL INFORMATION IS PROVIDED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 14742 | COMPR SRS 50MM DST HUM BDY RT | PROSTHESIS, SHOULDER | JDC | ZIMMER BIOMET, INC. | N/A | 213040 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 53 YR | Required Intervention |