FDA Adverse Event Malfunction Summary report: N

PANEL PHOENIX NMIC/ID-485

MDR report key: 23619217 · Received November 21, 2025

Report

Report Number
1119779-2025-05450
Event Type
Malfunction
Date Received
November 21, 2025
Date of Event
October 3, 2025
Report Date
November 21, 2025
Manufacturer
BECTON DICKINSON & CO. (SPARKS)
Product Code
LON
UDI-DI
00382904495268
PMA / PMN Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CI
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

E1. INITIAL REPORTER FACILITY NAME: (B)(6). A VALID LOT NUMBER WAS NOT REPORTED; HOWEVER, A POTENTIAL LOT NUMBER WAS PROVIDED. THE INFORMATION FOR THAT NUMBER IS AS FOLLOWS: D4. MEDICAL DEVICE LOT #:1051750. D4. MEDICAL DEVICE EXPIRATION DATE: UNKNOWN. H4. DEVICE MANUFACTURE DATE: UNKNOWN. H3. A DEVICE EVALUATION IS ANTICIPATED BUT HAS NOT YET BEGUN. UPON COMPLETION OF THE INVESTIGATION, A SUPPLEMENTAL REPORT WILL BE FILED.

Description of Event or Problem · 0

IT WAS REPORTED WHILE USING THE PANEL PHOENIX NMIC/ID-485 A PATIENT ISOLATE (ESCHERICHIA COLI) DID NOT REPORT AS EXTENDED SPECTRUM BETA-LACTAMASE (ESBL) POSITIVE. THE USER STATED THEY PERFORMED IMMUNOCHROMATOGRAPHIC STUDY FOR OXA-48, KLEBSIELLA PNEUMONIAE CARBAPENEMASE (KPC), NEW DELHI METALLO-BETA-LACTAMASE (NDM), VERONA INTEGRON-ENCODED METALLO-BETA-LACTAMASE (VIM), IMIPENEMASE (IMP) AND KIRBY BAUER TESTING. THE RESULTS WERE NEGATIVE FOR CARBAPENEMASE AND ESBL NEGATIVE. NO HEALTH IMPACT OR CONSEQUENCE REPORTED. REPORT 3 OF 3.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2076459 PANEL PHOENIX NMIC/ID-485 SYSTEM, TEST, AUTOMATED, ANTIMICROBIAL SUSCEPTIBILITY, SHORT INCUBATION LON BECTON DICKINSON & CO. (SPARKS) 1051750 00382904495268

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown