MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-03-25 for SMITHS MEDICAL LEVEL 1 HOTLINE LOW FLOW SYSTEMS CON-HL-90 manufactured by Smiths Medical Asd, Inc..
[184997244]
One fluid warmer was received for evaluation. Visual inspection of the device found it to be in good physical condition. The device was filled with water, fitted with temp check and powered on with attached line cord. The float switch alarm was triggered which happens when the water level drops too low-contrary to the customer complaint. In this investigation, the reported customer complaint has not been confirmed.
Patient Sequence No: 1, Text Type: N, H10
[184997245]
Information was received that a smiths medical level 1 hotline low flow system had level detector alarm. No adverse effects reported.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3012307300-2020-02399 |
| MDR Report Key | 9881592 |
| Report Source | USER FACILITY |
| Date Received | 2020-03-25 |
| Date of Report | 2020-03-23 |
| Date Mfgr Received | 2019-06-04 |
| Date Added to Maude | 2020-03-25 |
| 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 G1 | SMITHS MEDICAL ASD, INC. |
| Manufacturer Street | 3350 GRANADA AVENUE NORTH SUITE 100 |
| Manufacturer City | OAKDALE, MN |
| Manufacturer Country | US |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | SMITHS MEDICAL LEVEL 1 HOTLINE LOW FLOW SYSTEMS |
| Generic Name | WARMER, BLOOD, NON-ELECTROMAGNETIC RADIATION |
| Product Code | BSB |
| Date Received | 2020-03-25 |
| Returned To Mfg | 2019-06-05 |
| Catalog Number | CON-HL-90 |
| Device Availability | R |
| Device Eval'ed by Mfgr | Y |
| 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 | 2020-03-25 |