MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-07-17 for 1ML PURPLE ORAL SYRINGE STRL 401SG manufactured by Covidien.
Report Number | 1915484-2019-01062 |
MDR Report Key | 8799213 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2019-07-17 |
Date of Report | 2019-07-17 |
Date of Event | 2019-07-09 |
Date Mfgr Received | 2019-07-09 |
Date Added to Maude | 2019-07-17 |
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 | 1222 SHERWOOD RD |
Manufacturer City | NORFOLK NE 68701 |
Manufacturer Country | US |
Manufacturer Postal Code | 68701 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | 1ML PURPLE ORAL SYRINGE STRL |
Generic Name | CONTAINER, LIQUID MEDICATION, GRADUATED |
Product Code | KYW |
Date Received | 2019-07-17 |
Model Number | 401SG |
Catalog Number | 401SG |
Lot Number | 909849X |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COVIDIEN |
Manufacturer Address | 1222 SHERWOOD RD NORFOLK NE 68701 US 68701 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2019-07-17 |