FDA Adverse Event Malfunction Summary report: N

INSYTE AUTOG BC

MDR report key: 23129437 · Received September 23, 2025

Report

Report Number
1710034-2025-01558
Event Type
Malfunction
Date Received
September 23, 2025
Date of Event
September 9, 2025
Report Date
October 22, 2025
Manufacturer
BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.
Product Code
FOZ
PMA / PMN Number
K201075
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

OUR QUALITY ENGINEER INSPECTED THE SAMPLES SUBMITTED FOR EVALUATION. YOUR REPORT OF NEEDLE RETRACTION ISSUES COULD NOT BE CONFIRMED FROM THE 13 REPRESENTATIVE 22G INSYTE AUTOGUARD UNITS THAT WERE RECEIVED IN SEALED PACKAGING FROM LOT #5092496. A FUNCTIONAL TEST REVEALED THAT EACH NEEDLE FULLY RETRACTED WITHOUT RESISTANCE OR DELAY WHEN THE SAFETY MECHANISM WAS ACTIVATED. A DEVICE HISTORY RECORD REVIEW SHOWED NO NON-CONFORMANCES ASSOCIATED WITH THIS ISSUE DURING THE PRODUCTION OF THIS BATCH. HOWEVER, A TREND WAS IDENTIFIED FOR THE REPORTED FAILURE AND CORRECTIVE ACTIONS HAVE BEEN IMPLEMENTED TO INVESTIGATE THIS TYPE OF INCIDENT AND IDENTIFY THE ROOT CAUSE.

Additional Manufacturer Narrative · 0

H.3. A FOLLOW UP MDR WILL BE SUBMITTED IF ADDITIONAL INFORMATION, A DEVICE EVALUATION, OR A DEVICE HISTORY REVIEW IS COMPLETED.

Description of Event or Problem · 0

NO NEW INFORMATION.

Description of Event or Problem · 0

INJURIES OR ADVERSE EVENT: NO REPORTED ISSUE: WE HAVE HAD ISSUES WITH OUR IV NEEDLES NOT RETRACTING WHEN WE HIT THE BUTTON FOR THE RELEASE. GENERALLY, WITH WIGGLING WE HAVE BEEN ABLE TO GET IT TO RETRACT. HOWEVER, TODAY WE COULD NOT GET IT TO RETRACT AT ALL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
201620 INSYTE AUTOG BC PERIPHERAL IV CATHETERS FOZ BECTON DICKINSON INFUSION THERAPY SYSTEMS INC. 5092496

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown