MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-01-28 for SMITHS MEDICAL LEVEL 1 HOTLINE DISPOSABLE manufactured by Smiths Medical Asd, Inc..
[177370648]
Information was received that a smiths medical level 1 hotline low flow system tubing set not being accepted by fluid warmer. Incident was reported to have occurred while in use with a patient, and that no injury occurred.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3012307300-2020-00815 |
MDR Report Key | 9639555 |
Report Source | USER FACILITY |
Date Received | 2020-01-28 |
Date of Report | 2020-01-28 |
Date Mfgr Received | 2019-12-30 |
Device Manufacturer Date | 2019-04-02 |
Date Added to Maude | 2020-01-28 |
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 G1 | SMITHS MEDICAL ASD, INC. |
Manufacturer Street | 6000 NATHAN LANE N |
Manufacturer City | MINNEAPOLIS MN 55442 |
Manufacturer Country | US |
Manufacturer Postal Code | 55442 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SMITHS MEDICAL LEVEL 1 HOTLINE DISPOSABLE |
Generic Name | TUBING, FLUID DELIVERY |
Product Code | FPK |
Date Received | 2020-01-28 |
Device Availability | N |
Device Eval'ed by Mfgr | R |
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 | 2020-01-28 |