MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-06-21 for ARGYLE 8888750018 manufactured by Covidien.
[78235472]
Patient Sequence No: 1, Text Type: N, H10
[78235473]
The customer states that 9 units arrived with kinked tubing.
Patient Sequence No: 1, Text Type: D, B5
[135209175]
If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1282497-2017-05183 |
MDR Report Key | 6657015 |
Date Received | 2017-06-21 |
Date of Report | 2018-10-05 |
Date of Event | 2017-05-30 |
Date Mfgr Received | 2018-08-08 |
Date Added to Maude | 2017-06-21 |
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 | BOULEVARD INSURGENTES 19030 |
Manufacturer City | TIJUANA 22225 |
Manufacturer Country | MX |
Manufacturer Postal Code | 22225 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | ARGYLE |
Generic Name | CATHETER (GASTRIC, COLONIC, ETC.), IRRIGATION AND ASPIRATION |
Product Code | KDH |
Date Received | 2017-06-21 |
Model Number | 8888750018 |
Catalog Number | 8888750018 |
Lot Number | 170620003 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COVIDIEN |
Manufacturer Address | BOULEVARD INSURGENTES 19030 TIJUANA 22225 MX 22225 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2017-06-21 |