MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor report with the FDA on 2020-03-31 for CADD MS3 GRAY SLATE 7400 21-7411-51 manufactured by Smiths Medical Asd,inc.
[185922809]
Investigation completed on a smith medical cadd ms3 pump. Investigation revealed a short summary on event of alarming batteries are weak were related to motor issue. Other issues were found with device; s196 c294 r119. This issues were not revealed but repaired. Motor was repaired. A dhr review was performed subsequent to the manufacturing of the device and prior to its release. No problems or issues were identified during this dhr review.
Patient Sequence No: 1, Text Type: N, H10
[185922810]
?information received a smiths medical cadd ms3 gray slate pump is beeping and alarming, revealing on screen the batteries are weak .
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3012307300-2020-02442 |
MDR Report Key | 9908330 |
Report Source | DISTRIBUTOR |
Date Received | 2020-03-31 |
Date of Report | 2020-03-31 |
Date Mfgr Received | 2020-03-03 |
Device Manufacturer Date | 2016-08-17 |
Date Added to Maude | 2020-03-31 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | DAVE HALVERSON |
Manufacturer Street | 6000 LANE N |
Manufacturer City | MINNEAPOLIS, MN |
Manufacturer Country | US |
Manufacturer Phone | 3833310 |
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 | CADD MS3 GRAY SLATE |
Generic Name | PUMP, INFUSION |
Product Code | FRN |
Date Received | 2020-03-31 |
Returned To Mfg | 2020-03-09 |
Model Number | 7400 |
Catalog Number | 21-7411-51 |
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 LANE N MINNEAPOLIS, MN US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-31 |