FDA Adverse Event Malfunction Summary report: N

INTERMATE

MDR report key: 2963463 · Received February 15, 2013

Report

Report Number
1416980-2013-03915
Event Type
Malfunction
Date Received
February 15, 2013
Date of Event
January 1, 2013
Report Date
January 22, 2013
Manufacturer
BAXTER HEALTHCARE - IRVINE
Product Code
FRN
PMA / PMN Number
K910425
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
HEALTH PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

(B)(4). ONE SAMPLE WAS RECEIVED FOR EVALUATION. A BATCH REVIEW REVEALED PRODUCT MET ALL OF THE ACCEPTANCE CRITERIA FOR RELEASE. THE REPORTED CONDITION OF A RUPTURED RESERVOIR WAS CONFIRMED. VISUAL EXAMINATION OF THE UNIT DETERMINED THAT THE BLADDER RUPTURED IN A FOOTED POSITION. THE ROOT CAUSE COULD NOT BE DETERMINED. NO REPAIR WAS DONE, AS THIS IS A SINGLE-USE DEVICE WHICH WILL BE DISCARDED. NO OTHER OBSERVATIONS WERE NOTED ON THE UNIT. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A FOLLOW-UP WILL BE SUBMITTED. THE BATCH REVIEW REVEALED THAT ALL OF THE ACCEPTANCE CRITERIA WERE MET TO RELEASE THE LOT. THERE WERE NO NON-CONFORMANCES, FAILURES, REWORK, OR DEVIATIONS RELATED TO THE LOT. THERE WERE NO CHANGES TO SPECIFICATIONS, TEST METHODS, PROCESS, EQUIPMENT, OR RAW MATERIALS THAT COULD BE ASSOCIATED WITH THE REPORTED CONDITION. IF ADDITIONAL RELEVANT INFORMATION BECOMES AVAILABLE, A FOLLOW-UP WILL BE SUBMITTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT AN INTERMATE HAD A RESERVOIR RUPTURE AT THE END OF INFUSION. THE DEVICE WAS FILLED WITH A SOLUTION OF UNKNOWN CORTICOID DRUG. THERE WAS PATIENT INVOLVEMENT, BUT 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
69244 INTERMATE PUMP, INFUSION FRN BAXTER HEALTHCARE - IRVINE 12A064

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN CORTICOID DRUG