MAUDE Adverse Event Report: MAQUET CARDIOVASCULAR, LLC 30MM HEMA PLAT ANGLED 4 BR WDV AORTIC GRAFT; VASXCULAR GRAFT

Model Number M00202175730AP0

Device Problem Material Discolored (1170)

Patient Problem No Information (3190)

Event Date 03/18/2015

Event Type  malfunction  

Event Description

The hosp reported that there were yellow stains inside the 30mm hema plat angled 4 br wdv aortic graft.A replacement device was used to complete the procedure.The hosp did not report any pt effects.

Manufacturer Narrative

The device has not yet been returned to maquet cardiac surgery for eval.We are following up with the customer for the return of the device.A supplemental report will be submitted if the device is received.A lot history record review was completed for the reported product lot number.There was no nonconformance recorded in the lot history.(b)(4).

• Brand Name: 30MM HEMA PLAT ANGLED 4 BR WDV AORTIC GRAFT
• Type of Device: VASXCULAR GRAFT
• Manufacturer (Section D): MAQUET CARDIOVASCULAR, LLC; wayne NJ
• Manufacturer (Section G): MAQUET CARDIOVASCULAR, LLC; 45 barbour pond drive; wayne NJ 07470
• Manufacturer Contact: tina evancho ; 45 barbour pond drive; wayne, NJ 07470 ; 9737097265
• MDR Report Key: 4693011
• MDR Text Key: 5647815
• Report Number: 2242352-2015-00291
• Device Sequence Number: 1
• Product Code: MAL
• Combination Product (y/n): N
• Reporter Country Code: IT
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Foreign,Health Professional,User Facility,Company Representative
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date: 03/19/2015

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 04/13/2015
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Expiration Date: 02/28/2019
• Device Model Number: M00202175730AP0
• Device Lot Number: 25093479
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 03/19/2015
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 02/01/2014
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1