METRX CURRETTE *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2009-05-22 for METRX CURRETTE * manufactured by Medtronic, Inc..

Event Text Entries

[15449452] The physician was using a currette through a minimally invasive tube when the currette broke.
Patient Sequence No: 1, Text Type: D, B5

MAUDE Entry Details

• Report Number: 1397039
• MDR Report Key: 1397039
• Date Received: 2009-05-22
• Date of Report: 2009-05-22
• Date of Event: 2009-05-19
• Report Date: 2009-05-22
• Date Reported to FDA: 2009-05-22
• Date Added to Maude: 2009-06-03
• Event Key: 0
• Report Source Code: User Facility report
• Manufacturer Link: N
• Number of Patients in Event: 0
• Adverse Event Flag: 3
• Product Problem Flag: 3
• Reprocessed and Reused Flag: 0
• Health Professional: 3
• Initial Report to FDA: 3
• Report to FDA: 3
• Event Location: 3
• Single Use: 0
• Previous Use Code: 0
• Event Type: 3
• Type of Report: 3

Device Details

• Brand Name: METRX CURRETTE
• Generic Name: CURETTE
• Product Code: FZS
• Date Received: 2009-05-22
• Model Number: *
• Catalog Number: *
• Lot Number: *
• ID Number: *
• Operator: PHYSICIAN
• Device Age: 1 DY
• Device Sequence No: 1
• Device Event Key: 0
• Manufacturer: MEDTRONIC, INC.
• Manufacturer Address: MEDTRONIC SOFAMOR DANEK USA, I 1800 PYRAMID PLACE MEMPHIS TN 38132 US 38132

Patients

Patient Number	Treatment	Outcome	Date
1	0		2009-05-22