FDA Adverse Event Malfunction Summary report: N

VISTA BASIC - IFVB

MDR report key: 5401782 · Received February 1, 2016

Report

Report Number
9610825-2016-00018
Event Type
Malfunction
Date Received
February 1, 2016
Report Date
January 22, 2016
Manufacturer
B. BRAUN MELSUNGEN AG
Product Code
FRN
PMA / PMN Number
K003029
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 0

EXEMPTION NUMBER E2011009. B. BRAUN MEDICAL INC. IS SUBMITTING A SINGLE REPORT ON BEHALF OF B. BRAUN MELSUNGEN (THE MANUFACTURER), AND B. BRAUN MEDICAL INC. (THE IMPORTER). THIS REPORT HAS BEEN IDENTIFIED AS B. BRAUN MELSUNGEN INTERNAL REPORT NUMBER (B)(4). THE DEVICE INVOLVED HAS NOT BEEN RECEIVED FOR EVALUATION AND THE INVESTIGATION IS ONGOING AT THIS TIME. A FOLLOW UP WILL BE SUBMITTED WHEN THE INVESTIGATION RESULTS BECOME AVAILABLE.

Additional Manufacturer Narrative · 0

EXEMPTION NUMBER E2011009. B. BRAUN MEDICAL INC. IS SUBMITTING A SINGLE REPORT ON BEHALF OF B. BRAUN MELSUNGEN (THE MANUFACTURER), AND B. BRAUN MEDICAL INC. (THE IMPORTER). THIS REPORT HAS BEEN IDENTIFIED AS B. BRAUN MEDICAL INTERNAL REPORT NUMBER (B)(4). THE VOLUMETRIC ACCURACY WAS TESTED THREE TIMES AT 250ML/HR AND 25ML AND THE PUMP TESTED IN SPECIFICATIONS. BASED ON THE RESULTS OF THE INVESTIGATION, THE PUMP OPERATED AS INTENDED. IF ADDITIONAL PERTINENT INFORMATION BECOMES AVAILABLE, A FOLLOW UP WILL BE SUBMITTED.

Description of Event or Problem · 0

AS REPORTED BY THE USER FACILITY: EVENT DESCRIPTION: CUSTOMER STATED, "THE PUMP DRIPS TOO FAST AND OVER INFUSED." CUSTOMER DENIES ANY PATIENT INJURY AND NO FURTHER INFORMATION AS TO THE INFUSION RATE OR EVENT DESCRIPTION WAS PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
61085 VISTA BASIC - IFVB INFUSION PUMP FRN B. BRAUN MELSUNGEN AG

Patients

Seq Age Sex Outcome Treatment
1