MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2015-01-29 for STATSPIN MP X00-004998-001 manufactured by Iris Intl.
[5351711]
Customer reported smoke from the unit.
Patient Sequence No: 1, Text Type: D, B5
[12805687]
The customer reported a burned lid latch solenoid on their statspin mp. There were no reports of exposure to the operator, impact to pt samples, smoke, or fires. The fire dept was not called. The unit is being returned to beckman coulter for further analysis.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 2023446-2015-00009 |
MDR Report Key | 4483462 |
Report Source | 07 |
Date Received | 2015-01-29 |
Date of Report | 2015-01-06 |
Date of Event | 2015-01-06 |
Date Mfgr Received | 2015-01-06 |
Device Manufacturer Date | 2013-02-01 |
Date Added to Maude | 2015-03-04 |
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 | 0 |
Event Location | 0 |
Manufacturer Contact | SUDHA GUPTA |
Manufacturer Street | 9172 ETON AVE. |
Manufacturer City | CHATSWORTH CA 91311 |
Manufacturer Country | US |
Manufacturer Postal | 91311 |
Manufacturer Phone | 8185277272 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | STATSPIN MP |
Generic Name | STATSPIN CENTRIFUGE |
Product Code | GKG |
Date Received | 2015-01-29 |
Returned To Mfg | 2014-12-11 |
Catalog Number | X00-004998-001 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | IRIS INTL |
Manufacturer Address | 9172 ETON AVE. CHATSWORTH CA 91311 US 91311 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2015-01-29 |