FDA Adverse Event Other Summary report: N

UNITIP CATHETER FOR HR CATHETER

MDR report key: 3761535 · Received April 11, 2014

Report

Report Number
MW5035710
Event Type
Other
Date Received
April 11, 2014
Date of Event
April 1, 2014
Report Date
April 9, 2014
Manufacturer
UNISENSOR USA, INC
Product Code
FFX
Report Source
Voluntary report
Reporter Location
CO, US
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

ON (B)(6), THE DOCTOR AT THE HOSP NOTICED THAT THE CLINICIAN WAS NOT DISINFECTING THE ANORECTAL PROBE AFTER USE. WHEN ASKED ABOUT THAT, SHE SAID THAT SHE HAD NOT BEEN TRAINED TO DISINFECT THE PROBE. HOWEVER, PRIOR TO THIS TIME, ON (B)(6), THE SANDHILL SALES REP HAD BEEN TO THE ACCOUNT AND PERFORMED TRAINING ON PROPER OPERATION INCLUDING CLEANING AND DISINFECTING OF THE PROBE. ON (B)(6) WHEN THE SALES REP WAS AGAIN AT THE ACCOUNT ON ROUTINE BUSINESS, THE DOCTOR SAID HE HAD DISCOVERED THAT THE CLINICIAN HAD NOT DISINFECTED THE PROBE AND FIVE DIFFERENT PTS' HAD STUDIES PERFORMED USING THIS PROBE. THUS, POTENTIAL INJURY, DUE TO CROSS CONTAMINATION OF PTS, IS POSSIBLE DUE TO USING THE CONTAMINATED ANORECTAL PROBE. THIS REPORT IS BEING SUBMITTED AS A MEDICAL DEVICE REPORT IN AN ABUNDANCE OF CAUTION. INITIAL NOTICE OF THE POTENTIAL FOR INJURY. RESULTS OF THE EVAL OF THE PTS AND THE PRODUCT HAVE NOT BEEN COMMUNICATED TO SANDHILL. THIS IS OUTSIDE OF THE CONTROL OF SANDHILL SINCE WE DO NOT HAVE ACCESS TO THIS INFO. EVAL (B)(4). (B)(6).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
219845 UNITIP CATHETER FOR HR CATHETER UNITIP HIGH RESOLUTION CATHETER 12F FFX UNISENSOR USA, INC K1232345-L5-121114-

Patients

Seq Age Sex Outcome Treatment
1