MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2019-06-25 for 2 GA ROTOR LID CONTAINER - RED 8970 manufactured by Covidien.
Report Number | 1424643-2019-00539 |
MDR Report Key | 8731458 |
Report Source | COMPANY REPRESENTATIVE,USER F |
Date Received | 2019-06-25 |
Date of Report | 2019-06-25 |
Date of Event | 2019-06-06 |
Date Mfgr Received | 2019-06-07 |
Date Added to Maude | 2019-06-25 |
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 | JILL SARAIVA |
Manufacturer Street | 15 HAMPSHIRE STREET |
Manufacturer City | MANSFIELD MA 02048 |
Manufacturer Country | US |
Manufacturer Postal | 02048 |
Manufacturer Phone | 5086183640 |
Manufacturer G1 | COVIDIEN |
Manufacturer Street | 815 TEK DRIVE |
Manufacturer City | CRYSTAL LAKE IL 600399002 |
Manufacturer Country | US |
Manufacturer Postal Code | 600399002 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | 2 GA ROTOR LID CONTAINER - RED |
Generic Name | CONTAINER, SHARPS |
Product Code | MMK |
Date Received | 2019-06-25 |
Model Number | 8970 |
Catalog Number | 8970 |
Lot Number | 19B33163 |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COVIDIEN |
Manufacturer Address | 815 TEK DRIVE CRYSTAL LAKE IL 600399002 US 600399002 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-06-25 |