MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other report with the FDA on 2019-06-13 for KERLIX STERILE GAUZE BANDAGE ROLLS UNKNOWN PRODUCT manufactured by Covidien.
Report Number | 1018120-2019-00367 |
MDR Report Key | 8697579 |
Report Source | OTHER |
Date Received | 2019-06-13 |
Date of Report | 2019-06-13 |
Date Mfgr Received | 2019-05-23 |
Date Added to Maude | 2019-06-13 |
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 | 1430 MARVIN GRIFFIN ROAD, PO B |
Manufacturer City | AUGUSTA GA 30906 |
Manufacturer Country | US |
Manufacturer Postal Code | 30906 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | KERLIX STERILE GAUZE BANDAGE ROLLS |
Generic Name | GAUZE/SPONGE,NONRESORBABLE FOR EXTERNAL USE |
Product Code | NAB |
Date Received | 2019-06-13 |
Model Number | UNKNOWN PRODUCT |
Catalog Number | UNKNOWN PRODUCT |
Lot Number | UNKNOWN |
Device Availability | * |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COVIDIEN |
Manufacturer Address | 1430 MARVIN GRIFFIN ROAD, PO B AUGUSTA GA 30906 US 30906 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Deathisabilit | 2019-06-13 |