FDA Adverse Event Malfunction Summary report: N

EASYPUMP II LT 65-130-S

MDR report key: 3063520 · Received April 12, 2013

Report

Report Number
3009089744-2013-00087
Event Type
Malfunction
Date Received
April 12, 2013
Report Date
April 12, 2013
Manufacturer
B. BRAUN MEDICAL PRODUCTION LTD.
Product Code
MEB
PMA / PMN Number
K081905
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE DEVICE IS CURRENTLY ON SHIPPING FROM THE CUSTOMER TO B. BRAUN (B)(4) FOR INVESTIGATION. A FOLLOW-UP REPORT WILL BE PROVIDED AFTER THE INSPECTION RESULTS ARE AVAILABLE.

Description of Event or Problem · 1

AS REPORTED BY THE USER FACILITY (TRANSLATION OF USER FACILITY INFORMATION BY BBM SALES ORGANIZATION IN (B)(6)) : SLOW FLOW RATE. PUMP DID NOT INFUSE THE CORRECT AMOUNT OF CYTOSTATICA, WAS NOT EMPTY AFTER TWO DAYS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
157805 EASYPUMP II LT 65-130-S ELASTOMERIC INFUSION PUMP MEB B. BRAUN MEDICAL PRODUCTION LTD. NA 2C1528EH11

Patients

Seq Age Sex Outcome Treatment
1 UNK Other