MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-04-27 for SILSPT12TA manufactured by Covidien, Formerly Us Surgical A Divison.
[44467580]
(b)(4). (b)(4) complaint was received during this report period. The 1 reported device is labeled for single use. The device was not reprocessed and reused. No remedial action was taken.
Patient Sequence No: 1, Text Type: N, H10
[44467581]
This report summarizes
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1219930-2016-00381 |
MDR Report Key | 5611855 |
Date Received | 2016-04-27 |
Date Added to Maude | 2016-04-27 |
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 | SHARON MURPHY |
Manufacturer Street | 60 MIDDLETOWN AVE |
Manufacturer City | NORTH HAVEN CT 06473 |
Manufacturer Country | US |
Manufacturer Postal | 06473 |
Manufacturer Phone | 2034925267 |
Manufacturer G1 | COVIDIEN, FORMERLY US SURGICAL A DIVISON |
Manufacturer Street | 60 MIDDLETOWN AVE |
Manufacturer City | NORTH HAVEN CT 06473 |
Manufacturer Country | US |
Manufacturer Postal Code | 06473 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Generic Name | ANOSCOPE AND ACCESSORIES |
Product Code | FER |
Date Received | 2016-04-27 |
Model Number | SILSPT12TA |
Catalog Number | SILSPT12TA |
Device Availability | * |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COVIDIEN, FORMERLY US SURGICAL A DIVISON |
Manufacturer Address | 60 MIDDLETOWN AVE NORTH HAVEN CT 06473 US 06473 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2016-04-27 |