ACTIVE ARTICULATION HIP SYSTEM ARTIC E1 HIP BRG 28X42MM
Report
- Report Number
- 0001825034-2025-00992
- Event Type
- Injury
- Date Received
- April 4, 2025
- Date of Event
- March 29, 2025
- Report Date
- April 9, 2025
- Manufacturer
- ZIMMER BIOMET, INC.
- Product Code
- LPH
- UDI-DI
- 00880304485044
- PMA / PMN Number
- K161190
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AS
- Reporter Occupation
- PHYSICIAN
- Health Professional
- Yes
Narratives
THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION. THE FOLLOWING SECTIONS WERE {UPDATE/CORRECTED}. VISUAL EXAMINATION OF THE PROVIDED PICTURE IDENTIFIED THE EXPLANTED IMPLANTS BUT COULD NOT BE USED TO CONFIRM THE COMPLAINT. DEVICE NOT RETURNED; FURTHER ANALYSIS CANNOT BE MADE. REVIEW OF THE DEVICE HISTORY RECORDS IDENTIFIED NO DEVIATIONS OR ANOMALIES DURING MANUFACTURING. RADIOGRAPHS WERE PROVIDED AND REVIEWED BY A HEALTH CARE PROFESSIONAL. REVIEW OF THE AVAILABLE RECORDS IDENTIFIED THE FOLLOWING: A SINGLE UNDATED IMAGE REVIEWED AND NOT SUBMITTED TO MMI DUE TO THE INABILITY TO CORRELATE THE IMAGE WITH THE ALLEGATION. A DEFINITIVE ROOT CAUSE CANNOT BE DETERMINED. THIS COMPLAINT CANNOT BE CONFIRMED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS.
(B)(4). D10: CAT#: 802202801, LOT#: 3172598 FEMORAL HEAD 12/14 TAPER 28 MM DIAMETER -3.5 NECK LENGTH. CAT#: 00833408402, LOT#: 65430489 CEMENT PRESSURIZER MEDIUM. CAT#: P0463048, LOT#: 0001799214 AVAN CMNTD SHELL SS 48MM. CAT#: 42.19.40, LOT#: 9999999999 COUNTERSUNK CANCELL SCR 6.5/40. CAT#: 42.19.30, LOT#: 9999999999 COUNTERSUNK CANCELL SCR 6.5/30. CAT#: 01.00191.250, LOT#: 3002257 B-S REINFORCMNT RING NEW 50 RT. CAT#: 00811400110, LOT#: 66348502 FEMORAL STEM 12/14 NECK TAPER EXT. OFFSET SIZE 1 130 MM STEM LENGTH. CAT#: 00801102024, LOT#: 66352085, ALLEN MEDULLARY CEMENT PLUGS 1-24 MM DIAMETER FLANGE/12 MM DIAMETER CORE STORE IN COOL DRY PLACE. G2: FOREIGN: AUSTRALIA. 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.
NO FURTHER INFORMATION AT THE TIME OF THIS REPORT.
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL HIP PROCEDURE. SUBSEQUENTLY, THE PATIENT WAS REVISED APPROXIMATELY 1 YEAR LATER DUE TO DISSOCIATION. THE HEAD AND BEARING DISASSOCIATED AND WERE REPLACED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 686591 | ACTIVE ARTICULATION HIP SYSTEM ARTIC E1 HIP BRG 28X42MM | PROSTHESIS, HIP | LPH | ZIMMER BIOMET, INC. | 66202329 | 00880304485044 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Male | Hospitalization| R | SEE H11 NARRATIVE. |