STATSPIN MP X00-003917-001

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2014-08-28 for STATSPIN MP X00-003917-001 manufactured by Iris International.

Event Text Entries

[21494288] Customer reported the unit was not spinning well.
Patient Sequence No: 1, Text Type: D, B5

[21685803] Inadequate spinning of samples was reported for the centrifuge. Customer had to spin multiple times to separate the tubes. No change to pt management or erroneous results were generated.
Patient Sequence No: 1, Text Type: N, H10

MAUDE Entry Details

• Report Number: 2023446-2014-00139
• MDR Report Key: 4102704
• Report Source: 05,06
• Date Received: 2014-08-28
• Date of Report: 2014-07-31
• Date of Event: 2014-07-31
• Date Mfgr Received: 2014-07-31
• Device Manufacturer Date: 2009-08-01
• Date Added to Maude: 2014-09-26
• 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

Device Details

• Brand Name: STATSPIN MP
• Generic Name: STATSPIN CENTRIFUGE
• Product Code: GKG
• Date Received: 2014-08-28
• Catalog Number: X00-003917-001
• 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 INTERNATIONAL
• Manufacturer Address: 9172 ETON AVE. CHATSWORTH CA 91311 US 91311

Patients

Patient Number	Treatment	Outcome	Date
1	0		2014-08-28