MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2018-10-25 for REAL SEAL manufactured by Sybronendo.
[125040512]
Specific patient information with regards to age, gender, weight was not provided. The patients required a re-treatment of the root canal. The product was not returned and no lot number was provided; therefore, no evaluation can be conducted.
Patient Sequence No: 1, Text Type: N, H10
[125040513]
A doctor alleged that while performing a resilon retreatment several findings were noted. The findings were indicated as black pigmentation, soft resilon material, necrotic smell, lesions, and infected.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2016150-2018-00058 |
| MDR Report Key | 8006441 |
| Report Source | HEALTH PROFESSIONAL |
| Date Received | 2018-10-25 |
| Date of Report | 2018-03-09 |
| Date of Event | 2018-02-01 |
| Date Mfgr Received | 2018-03-09 |
| Date Added to Maude | 2018-10-25 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 0 |
| Initial Report to FDA | 0 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MR. PAULO CALLE |
| Manufacturer Street | 1717 W COLLINS AVENUE |
| Manufacturer City | ORANGE CA 92867 |
| Manufacturer Country | US |
| Manufacturer Postal | 92867 |
| Manufacturer Phone | 7145167752 |
| Manufacturer G1 | SYBRONENDO |
| Manufacturer Street | 1332 SOUTH LONE HILL AVENUE |
| Manufacturer City | GLENDORA CA 91740 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 91740 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | REAL SEAL |
| Generic Name | ROOT CANAL FILLING, PRODUCT CODE: KIF |
| Product Code | KIF |
| Date Received | 2018-10-25 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | SYBRONENDO |
| Manufacturer Address | 1332 SOUTH LONE HILL AVENUE GLENDORA CA 91740 US 91740 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2018-10-25 |