FDA Adverse Event Malfunction Summary report: N

SPINNING SPIROS CLOSED MALE LUER

MDR report key: 8439267 · Received March 21, 2019

Report

Report Number
9617594-2019-00097
Event Type
Malfunction
Date Received
March 21, 2019
Date of Event
January 1, 2019
Report Date
February 28, 2019
Manufacturer
ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.
Product Code
FPA
UDI-DI
00887709036796
PMA / PMN Number
K082806
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

NO K7040-001 SPIROS PRODUCT SAMPLES, VIDEOS, OR PHOTOGRAPHS WERE RETURNED FOR INVESTIGATION. THE DHR FOR LOT 3244017 WAS REVIEWED AND THERE WERE NO RELEVANT NON-CONFORMANCES FOUND THAT WOULD HAVE CONTRIBUTED TO THE REPORTED COMPLAINT. A PROBABLE CAUSE CANNOT BE IDENTIFIED BASED ON THE INFORMATION THAT HAS BEEN PROVIDED.

Additional Manufacturer Narrative · 1

THE DEVICE IS AVAILABLE FOR EVALUATION. IT IS YET TO BE RECEIVED.

Description of Event or Problem · 1

THE EVENT OCCURRED ON AN UNKNOWN DATE AND INVOLVED TWO SPINNING SPIROS CLOSED MALE LUERS ATTACHED TO AN INFUSOR BOTTLE WHICH CAUSED A SPILL OF AN UNKNOWN CHEMOTHERAPY MEDICATION WHEN THE NURSE PLACED THE BOTTLE ON THE CHAIR SIDE TABLE. THE SPILL CAME INTO CONTACT WITH THE HEALTHCARE PROVIDER¿S GLOVES, WHICH WERE IMMEDIATELY REMOVED AND THE PROVIDER¿S HANDS WERE WASHED. THE CHEMO SPILL WAS CLEANED PER FACILITY PROTOCOL, THE PRODUCT WAS REPLACED, AND THE THERAPY WAS RESUMED. THERE WAS NO PATIENT INVOLVEMENT, NO ADVERSE EVENT, BUT THERE WAS A DELAY IN THERAPY AS ANOTHER BOTTLE HAD TO BE MIXED. THIS CAPTURES THE SECOND OF TWO DEVICES. NO ADDITIONAL INFORMATION WAS PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
234401 SPINNING SPIROS CLOSED MALE LUER SET, ADMINISTRATION, INTRAVASCULAR FPA ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V. 3244017 00887709036796

Patients

Seq Age Sex Outcome Treatment
1 UNSP CHEMOTHERAPY.| UNSP CHEMOTHERAPY