MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-09 for CC10522Z manufactured by Boston Scientific Neuromodulation.
[182743258]
A report was received that the patient experienced a localized rash at the needle site. The symptoms were red blotches, a reaction that looked like an insect bite, and itchiness weeks after the procedure. The device was not returned to bsn as it was discarded by the medical facility.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3006630150-2020-01079 |
MDR Report Key | 9808635 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-03-09 |
Date of Report | 2020-03-09 |
Date of Event | 2019-12-20 |
Date Mfgr Received | 2020-02-21 |
Date Added to Maude | 2020-03-09 |
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 | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | TALAR TAHMASIAN |
Manufacturer Street | 25155 RYE CANYON LOOP |
Manufacturer City | VALENCIA CA 91355 |
Manufacturer Country | US |
Manufacturer Postal | 91355 |
Manufacturer Phone | 6619494863 |
Manufacturer G1 | BOSTON SCIENTIFIC DE COSTA RICA S.R.L. |
Manufacturer City | ALAJUELA |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Generic Name | PROBE, RADIOFREQUENCY LESION |
Product Code | GXI |
Date Received | 2020-03-09 |
Model Number | CC10522Z |
Catalog Number | CC10522Z |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BOSTON SCIENTIFIC NEUROMODULATION |
Manufacturer Address | 25155 RYE CANYON LOOP VALENCIA CA 91355 US 91355 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2020-03-09 |