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 2020-03-17 for PORTEX? BLUE LINE ULTRA? TRACHEOSTOMY TUBE 100/813/070CZ manufactured by Smiths Medical Asd; Inc..
[183871924]
Information was received indicating that the inner cannula to a smiths medical portex? Blue line ultra? Tracheostomy tube was noted to be broken. There were no reported adverse effects.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3012307300-2020-02107 |
MDR Report Key | 9845352 |
Report Source | FOREIGN,USER FACILITY |
Date Received | 2020-03-17 |
Date of Report | 2020-03-17 |
Date Mfgr Received | 2020-02-19 |
Date Added to Maude | 2020-03-17 |
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 | DAVE HALVERSON |
Manufacturer Street | 6000 NATHAN LANE N |
Manufacturer City | MINNEAPOLIS,, MN |
Manufacturer Country | US |
Manufacturer Phone | 3833310 |
Manufacturer G1 | SMITHS MEDICAL CZECH REPUBLIC A. S. |
Manufacturer Street | OLOMOUCK? 306 |
Manufacturer City | HRANICE 1-MESTO, |
Manufacturer Country | EZ |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PORTEX? BLUE LINE ULTRA? TRACHEOSTOMY TUBE |
Generic Name | TUBE TRACHEOSTOMY AND TUBE CUFF |
Product Code | JOH |
Date Received | 2020-03-17 |
Returned To Mfg | 2020-02-21 |
Catalog Number | 100/813/070CZ |
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 US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-17 |