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 2020-01-08 for SHILEY 125-37-1 manufactured by Mallinckrodt Medical.
[188146169]
This event has been reassessed and found to be a non-mdr reportable complaint. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 8020889-2020-00001 |
MDR Report Key | 9564259 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-01-08 |
Date of Report | 2020-01-15 |
Date of Event | 2020-01-02 |
Date Mfgr Received | 2020-01-02 |
Device Manufacturer Date | 2017-02-24 |
Date Added to Maude | 2020-01-08 |
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 | AVI KLUGER |
Manufacturer Street | 5920 LONGBOW DRIVE |
Manufacturer City | BOULDER CO 80301 |
Manufacturer Country | US |
Manufacturer Postal | 80301 |
Manufacturer Phone | 3035306582 |
Manufacturer G1 | MALLINCKRODT MEDICAL |
Manufacturer Street | CORNAMADDY |
Manufacturer City | ATHLONE 3810 |
Manufacturer Postal Code | 3810 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SHILEY |
Generic Name | TUBE, BRONCHIAL (W/WO CONNECTOR) |
Product Code | BTS |
Date Received | 2020-01-08 |
Model Number | 125-37-1 |
Catalog Number | 125-37-1 |
Lot Number | 201702474X |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MALLINCKRODT MEDICAL |
Manufacturer Address | CORNAMADDY ATHLONE 3810 3810 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-01-08 |