FDA Adverse Event Malfunction Summary report: N

ACCESS

MDR report key: 5071380 · Received September 11, 2015

Report

Report Number
1416980-2015-35673
Event Type
Malfunction
Date Received
September 11, 2015
Date of Event
September 1, 2015
Report Date
September 15, 2015
Manufacturer
BAXTER HEALTHCARE - MALTA
Product Code
LJH
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
EI
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). A BATCH REVIEW WAS CONDUCTED AND THERE WERE NO DEVIATIONS FOUND RELATED TO THIS REPORTED CONDITION DURING THE MANUFACTURE OF THIS LOT. THE DEVICE WAS NOT RECEIVED FOR EVALUATION; THEREFORE, A DEVICE ANALYSIS COULD NOT BE COMPLETED. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Additional Manufacturer Narrative · 1

(B)(4). SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT A UROMATIC TUR ADMINISTRATION HAD A TIP COMING OFF WHEN IT WAS SPIKED TO A BAG. THERE WAS NO PATIENT INVOLVEMENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
602297 ACCESS SYSTEM, IRRIGATION, UROLOGICAL LJH BAXTER HEALTHCARE - MALTA 14K03V521

Patients

Seq Age Sex Outcome Treatment
1