MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-02-23 for MECTA SPECTRUM 5000Q SPECTRUM 5000 Q manufactured by Mecta Corporation.
[100888774]
Not possible to followup on the injury report.
Patient Sequence No: 1, Text Type: N, H10
[100888775]
Severe amnesia following ect treatments from (b)(6) for depression. Remains disabled after 10 years.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3020533-2018-00001 |
| MDR Report Key | 7294038 |
| Date Received | 2018-02-23 |
| Date of Event | 1999-12-20 |
| Date Mfgr Received | 2017-12-20 |
| Date Added to Maude | 2018-02-23 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 0 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 0 |
| Initial Report to FDA | 0 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MRS. ROBIN NICOL |
| Manufacturer Street | 19799 SW 95TH AVENUE SUITE B |
| Manufacturer City | TUALATIN OR 97062 |
| Manufacturer Country | US |
| Manufacturer Postal | 97062 |
| Manufacturer Phone | 5036126780 |
| Manufacturer G1 | MECTA CORPORATION |
| Manufacturer Street | 19799 SW 95TH AVENUE SUITE B |
| Manufacturer City | TUALATIN OR 97062 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 97062 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | MECTA SPECTRUM 5000Q |
| Generic Name | ECTDEVICE |
| Product Code | GXC |
| Date Received | 2018-02-23 |
| Model Number | SPECTRUM 5000 Q |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MECTA CORPORATION |
| Manufacturer Address | 19799 SW 95TH AVE. SUITE B TUALATIN OR 97062 US 97062 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2018-02-23 |