FDA Adverse Event Malfunction Summary report: N

BLOOD SET 4MM

MDR report key: 1873218 · Received October 18, 2010

Report

Report Number
6000001-2010-04218
Event Type
Malfunction
Date Received
October 18, 2010
Date of Event
October 1, 2010
Report Date
October 4, 2010
Manufacturer
BAXTER HEALTHCARE - MALTA
Product Code
BRZ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THIS DEVICE IS MANUFACTURED FOR DISTRIBUTION OUTSIDE OF THE UNITED STATES (US); THEREFORE, IT DOES NOT CONTAIN A US 510K NUMBER. HOWEVER, THIS MDR IS BEING SUBMITTED BECAUSE IT IS THE SAME AS OR SIMILAR TO A PRODUCT DISTRIBUTED WITHIN THE US.EVALUATION SUMMARY:THE REPORTED CONDITION OF A 4MM BLOOD SET WHICH WAS FOUND TO HAVE GREASE INSIDE ITS DRIP CHAMBER WAS CONFIRMED DURING PRODUCT EVALUATION AS THE DRIP CHAMBER'S PLASTIC MATERIAL BEING CLOUDY. THIS CONDITION WAS CAUSED BY A MIGRATION OF STEARATE, ONE OF THE CONSTITUENTS OF THE PLASTIC MATERIAL COMPRISING THE SET. THIS DEVICE IS A SINGLE USE DEVICE AND WILL BE DISCARDED. 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

IT WAS REPORTED TO BAXTER (B)(4) THAT A 4MM BLOOD SET WAS FOUND TO HAVE GREASE INSIDE ITS DRIP CHAMBER, THEREBY CONTAMINATING THE STERILE FLUID PATH. THIS CONDITION WAS DISCOVERED BEFORE USE. THERE WAS NO PATIENT INJURY OR MEDICAL INTERVENTION NECESSARY AS THIS EVENT DID NOT OCCUR DURING PATIENT USE. NO ADDITIONAL INFORMATION IS AVAILABLE.A 10 4MM BLOOD SETS, ALL LOT # 08C22V792, WERE REPORTED TO HAVE GREASE IN THEIR DRIP CHAMBERS. THIS MEDWATCH IS FOR SET 10 OF 10.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BLOOD SET 4MM SET, BLOOD TRANSFUSION BRZ BAXTER HEALTHCARE - MALTA 08C22V792

Patients

Seq Age Sex Outcome Treatment
1