MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-01-03 for CADD SOLIS HPCA 2110 21-2111-0300-01 manufactured by Smiths Medical Asd, Inc.
[175848788]
It was reported that the delivery rate of the pump was inaccurate. No patient injury or complications were reported in relation to this event.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3012307300-2020-00131 |
MDR Report Key | 9548559 |
Report Source | USER FACILITY |
Date Received | 2020-01-03 |
Date of Report | 2020-02-21 |
Date of Event | 2019-11-29 |
Date Mfgr Received | 2020-01-22 |
Device Manufacturer Date | 2014-05-07 |
Date Added to Maude | 2020-01-03 |
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 NORTH |
Manufacturer City | MINNEAPOLIS MN 55442 |
Manufacturer Country | US |
Manufacturer Postal | 55442 |
Manufacturer G1 | SMITHS MEDICAL ASD, INC |
Manufacturer Street | 3350 GRANADA AVENUE NORTH SUITE 100 |
Manufacturer City | OAKDALE MN 55128 |
Manufacturer Country | US |
Manufacturer Postal Code | 55128 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CADD SOLIS HPCA |
Generic Name | PUMP, INFUSION, PCA |
Product Code | MEA |
Date Received | 2020-01-03 |
Returned To Mfg | 2020-01-27 |
Model Number | 2110 |
Catalog Number | 21-2111-0300-01 |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SMITHS MEDICAL ASD, INC |
Manufacturer Address | 6000 NATHAN LANE NORTH MINNEAPOLIS MN 55442 US 55442 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-01-03 |