FDA Adverse Event Malfunction Summary report: N

CE INFUSOR LV10, 12 PACK

MDR report key: 1761121 · Received July 19, 2010

Report

Report Number
6000001-2010-01751
Event Type
Malfunction
Date Received
July 19, 2010
Date of Event
June 30, 2010
Report Date
July 1, 2010
Manufacturer
BAXTER HEALTHCARE - IRVINE
Product Code
MEB
PMA / PMN Number
K071222
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AS
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE CUSTOMER DID NOT SEND THE DEVICE TO BAXTER FOR EVALUATION. THEREFORE, THE REPORTED CONDITION OF THE DEVICE DELIVERING FASTER THAN INTENDED COULD NOT BE CONFIRMED. SHOULD THE SAMPLE AND/OR ADDITIONAL INFORMATION BE RECEIVED, A FOLLOW-UP MEDWATCH WILL BE SUBMITTED.

Additional Manufacturer Narrative · 1

(B)(4). ADDITIONAL INFORMATION:A BATCH REVIEW WAS PERFORMED FINDING THAT NO EXCEPTION/NON-CONFORMANCE REPORTS WERE DOCUMENTED FOR THIS LOT. ALL RELEASE CRITERIA WERE MET FOR THE BUILD OF THE LOT.

Description of Event or Problem · 1

PER THE CLINIC, THE PATIENT EXPERIENCED A PERFORMANCE DECREMENT, RESULTING IN THE DECISION TO EXPLANT THE DEVICE. THE DEVICE WAS EXPLANTED (B)(6), 2009, AND THE PATIENT WAS REIMPLANTED WITH A NEW DEVICE DURING THE SAME SURGERY.

Description of Event or Problem · 1

IT WAS REPORTED TO BAXTER (B)(4) THAT AN INFUSOR LV 10 DEVICE DELIVERED IN A FASTER THAN EXPECTED TIME DURING A PATIENT INFUSION. THE PUMP FULLY INFUSED A SOLUTION OF 8 GRAMS OF FLUCLOXACILLIN AND 240ML OF NORMAL SALINE 2-3 HOURS EARLIER THAN INTENDED. THERE WAS NO REPORT OF PATIENT INJURY, MEDICAL INTERVENTION NECESSARY, OR ADVERSE REACTION IN ASSOCIATION WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CE INFUSOR LV10, 12 PACK PUMP, INFUSION, ELASTOMERIC MEB BAXTER HEALTHCARE - IRVINE 10C057

Patients

Seq Age Sex Outcome Treatment
1