MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,user facility report with the FDA on 2019-10-23 for PORTEX? ENDOTRACHEAL TUBE 100/150/080 manufactured by Smiths Medical Asd; Inc..
Report Number | 3012307300-2019-05395 |
MDR Report Key | 9226705 |
Report Source | FOREIGN,USER FACILITY |
Date Received | 2019-10-23 |
Date of Report | 2019-10-22 |
Date of Event | 2019-07-15 |
Date Mfgr Received | 2019-07-25 |
Device Manufacturer Date | 2019-03-12 |
Date Added to Maude | 2019-10-23 |
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 | DAVE HALVERSON |
Manufacturer Street | 6000 NATHAN LANE N |
Manufacturer City | MINNEAPOLIS, MN 55442 |
Manufacturer Country | US |
Manufacturer Postal | 55442 |
Manufacturer Phone | 7633833310 |
Manufacturer G1 | SMITHS MEDICAL INTERNATIONAL LTD. |
Manufacturer Street | BOUNDARY ROAD |
Manufacturer City | HYTHE, CT216JL |
Manufacturer Country | UK |
Manufacturer Postal Code | CT21 6JL |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PORTEX? ENDOTRACHEAL TUBE |
Generic Name | TUBE, TRACHEOSTOMY (W/WO CONNECTOR) |
Product Code | BTO |
Date Received | 2019-10-23 |
Returned To Mfg | 2019-08-09 |
Catalog Number | 100/150/080 |
Lot Number | 19022580 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SMITHS MEDICAL ASD; INC. |
Manufacturer Address | 6000 NATHAN LANE N MINNEAPOLIS, MN 55442 US 55442 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Life Threatening; 2. Required No Informationntervention | 2019-10-23 |