MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-10-19 for MICROBORE EXTENSION SET, 60IN 60ES manufactured by Covidien.
[57923009]
An investigation is currently underway. Upon completion, the results will be forwarded.
Patient Sequence No: 1, Text Type: N, H10
[57923010]
It was reported to covidien on 10/14/2016 that a customer had an issue with an extension set. The customer reports that the extension set is bonded together and will not allow fluids to pass.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9612030-2016-00535 |
MDR Report Key | 6041940 |
Date Received | 2016-10-19 |
Date of Report | 2016-10-14 |
Date of Event | 2016-10-14 |
Date Mfgr Received | 2016-10-14 |
Date Added to Maude | 2016-10-19 |
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 | EDWARD ALMEIDA |
Manufacturer Street | 15 HAMPSHIRE STREET |
Manufacturer City | MANSFIELD MA 02048 |
Manufacturer Country | US |
Manufacturer Postal | 02048 |
Manufacturer Phone | 5084524151 |
Manufacturer G1 | COVIDIEN |
Manufacturer Street | CALLE 9 SUR NO. 125 CUIDAD INDUSTRIAL |
Manufacturer City | TIJUANA |
Manufacturer Country | MX |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | MICROBORE EXTENSION SET, 60IN |
Generic Name | EXTENSION SET |
Product Code | FPK |
Date Received | 2016-10-19 |
Model Number | 60ES |
Catalog Number | 60ES |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COVIDIEN |
Manufacturer Address | CALLE 9 SUR NO. 125 CUIDAD INDUSTRIAL TIJUANA MX |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2016-10-19 |