ANATOMICS STARPORE EAR IMPLANT
Report
- Report Number
- 3007630408-2023-00014
- Event Type
- Injury
- Date Received
- August 3, 2023
- Report Date
- August 2, 2023
- Manufacturer
- ANATOMICS PTY LTD
- Product Code
- JOF
- PMA / PMN Number
- NANA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- US
- Reporter Occupation
- OTHER
- Health Professional
- N
Narratives
DEVICES REQUIRE PATHOLOGY TESTINGS OR BE RETURNED TO MANUFACTURER TO AID WITH THE INVESTIGATION. IF ADDITIONAL INFORMATION IS RECEIVED FROM THE CUSTOMERS REGARDING THE EVENT, IT WILL BE REPORTED IN A SUPPLEMENTAL REPORT. IMPLANTS' TRACEABILITY WERE CHECKED AND FOUND TO HAVE NO PROCESS NOR PRODUCT NON-CONFORMITIES. SAMPLES FROM UNUSED (STOCK-ON-HAND) SIMILAR IMPLANTS MANUFACTURED AT A SIMILAR TIME POINT USING THE SAME PROCESS AND MATERIALS AS THE IMPLANTS IN QUESTION WERE SENT FOR ROUTINE ANALYSES (ENDOTOXIN AND STERILITY TESTINGS). THE TESTINGS SHOW SATISFACTORY RESULTS AS FOLLOWS: ENDOTOXIN LEVEL: <5 EU/DEVICE (LIMIT: 20 EU/DEVICE); STERILITY: NO VISIBLE GROWTH OF MICROORGANISMS. CONCLUSION TO DATE: NO ANOMALIES FOUND ON THE DEVICES.
THIS SUPPLEMENTAL REPORT IS TO CORRECT BLOCK H.1 INFORMATION AS PER CDRH'S REQUEST.
SURGEON ADVISED TO EXPLANT AND REPLACE STARPORE EARS BECAUSE OF NON-SPECIFIC SWELLING. THE PATIENT IS EXPECTED HAVE A SATISFACTORY RECOVERY JUST AS OTHER PATIENTS HAD.
SURGEON ADVISED TO EXPLANT AND REPLACE STARPORE EARS BECAUSE OF NON-SPECIFIC SWELLING. THE PATIENT IS EXPECTED HAVE A SATISFACTORY RECOVERY JUST AS OTHER PATIENTS HAD.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 318444 | ANATOMICS STARPORE EAR IMPLANT | POLYMER, ENT SYNTHETIC, POROUS POLYETHYLENE | JOF | ANATOMICS PTY LTD |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Prefer Not To Disclose | Other| R |