N-TRALIG INTRLGMNTRY SYRG
Report
- Report Number
- 2523190-2017-00121
- Event Type
- Malfunction
- Date Received
- November 1, 2017
- Date of Event
- September 28, 2017
- Report Date
- October 5, 2017
- Manufacturer
- INTEGRA YORK, PA INC.
- Product Code
- EJI
- PMA / PMN Number
- K142414
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- DENTIST
Narratives
ON (B)(6) 2017 INTEGRA INVESTIGATION COMPLETED. METHOD: FAILURE ANALYSIS, DEVICE HISTORY EVALUATION RESULTS: FAILURE ANALYSIS - THE CUSTOMER SUPPLIED PICTURES INDICATE NECROTIC TISSUE AT INJECTION SITE. THE CAUSE FOR THE NECROTIC TISSUE CAN NOT BE DETERMINED AS THE NEEDLE, LIDOCAINE, AND PROCESS DURING THE PROCEDURE IS NOT KNOWN. THE COMPLAINT IS CONFIRMED. DEVICE HISTORY EVALUATION - ANY APPLICABLE NONCONFORMING PRODUCT REPORT / NONCONFORMING MATERIAL REPORT HISTORY: NONE ANY APPLICABLE VARIANCE AUTHORIZATION / DEVIATION HISTORY: NONE ANY APPLICABLE ENGINEERING CHANGE ORDER / MANUFACTURING CHANGE ORDER HISTORY: NONE ANY APPLICABLE CORRECTIVE ACTION PREVENTIVE ACTION HISTORY: NONE HEALTH HAZARD EVALUATION HISTORY: NONE CONCLUSION: THE CUSTOMER SUPPLIED PICTURES INDICATE NECROTIC TISSUE AT INJECTION SITE. ROOT CAUSE UNDETERMINED. THERE HAS BEEN NO MANUFACTURING DEFICIENCY IDENTIFIED.
DOCTOR INITIALLY REPORTS THE SYRINGE CREATED NECROTIC TISSUE AT THE INJECTION SITE. ON (B)(6) 2017 DOCTOR REPORTS ANESTHETIC USED: SEPTOCAINE 1:200,000 - APPROXIMATELY 1/3-1/2 CARPULE INJECTED AT CERVICAL OF FACIAL SURFACE OF TOOTH AT GUM LINE UNDER PRESSURE AT 3 SITES MESIAL PROXIMAL, FACIAL, DISTAL PROXIMAL CHLORHEXADINE RINSE CLEARED UP THE AREA. AREA RESOLVED WITHOUT FURTHER INCIDENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 773021 | N-TRALIG INTRLGMNTRY SYRG | M51 - GENERAL DENTISTRY | EJI | INTEGRA YORK, PA INC. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 33 YR |