ECHO BI-METRIC HIP SYSTEM
Report
- Report Number
- 0001822565-2025-00800
- Event Type
- Injury
- Date Received
- March 28, 2025
- Report Date
- April 10, 2025
- Manufacturer
- ZIMMER BIOMET, INC.
- Product Code
- KWA
- PMA / PMN Number
- K070274
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- PHYSICIAN
- Health Professional
- Yes
Narratives
(B)(4). D10: CAT: 12-115111 LOT: 2965002 CER BIOLOXD MOD HD 28MM +3 NK CAT: 110010268 LOT: 6463667 G7 OSSEOTI MULTIHOLE 60MM G CAT: 110024465 LOT: 665360 G7 DUAL MOBILITY LINER 46MM G H6: PROPOSED COMPONENT COODE: SUGGESTED COMPONENT CODE: MECHANICAL (G04) - STEM THE CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED TO ZIMMER BIOMET FOR INVESTIGATION, AS ITS LOCATION IS UNKNOWN. THE INVESTIGATION IS IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED.
UPON RECEIVING ADDITIONAL INFORMATION OF THE REPORTED EVENT, IT WAS DETERMINED TO BE NOT REPORTABLE AS THIS PRODUCT WAS NOT INVOLVED IN THE EVENT. THE INITIAL REPORT SHOULD BE VOIDED.
IT WAS REPORTED THAT APPROXIMATELY FIVE YEARS POST-IMPLANTATION, THE PATIENT WILL BE REVISED DUE TO UNKNOWN REASONS. IT IS UNKNOWN IF A REVISION HAS TAKEN PLACE. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
UPON RECEIVING ADDITIONAL INFORMATION OF THE REPORTED EVENT, IT WAS DETERMINED TO BE NOT REPORTABLE AS THIS PRODUCT WAS NOT INVOLVED IN THE EVENT. THE INITIAL REPORT SHOULD BE VOIDED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1437940 | ECHO BI-METRIC HIP SYSTEM | PROSTHESIS, HIP | KWA | ZIMMER BIOMET, INC. | 441380 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Male | Other | SEE H11 NARRATIVE |