FDA Adverse Event Malfunction Summary report: N

PANEL PHOENIX NMIC-312

MDR report key: 24638617 · Received March 19, 2026

Report

Report Number
1119779-2026-00423
Event Type
Malfunction
Date Received
March 19, 2026
Date of Event
February 23, 2026
Report Date
March 18, 2026
Manufacturer
BECTON DICKINSON & CO. (SPARKS)
Product Code
LON
UDI-DI
30382904490820
PMA / PMN Number
SEE H11
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MD, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THERE WERE MULTIPLE 510K NUMBERS REPORTED TO BE INVOLVED. THE INFORMATION FOR THE ADDITIONAL 510K IS AS FOLLOWS: G4. PMA/510(K)#: K020322, K023444, K023634, K023858, K033458, K042932, K060214, K060257, K060444, K060447, K061327, K061355, K062207, K062944, K062945, K063486, K063573, K063811, K063824, K123404, K132674, K132909, K163637, K173252, K173523, K181665, AND K233986. 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-312 A PATIENT ISOLATE (ESCHERICHIA COLI) HAD RESISTANT TO ERTAPENEM AND MEROPENEM, AS WELL AS CEFEPIME, AVYCAZ (CEFTAZIDIME/AVIBACTAM), AND ZERBAXA (CEFTOLOZANE/TAZOBACTAM) DESPITE BEING SENSITIVE TO DRUGS LIKE AMPICILLIN, CEFTRIAXONE AND IMIPENEM. THE USER PERFORMED REPEAT TESTING GIVING SENSITIVE RESULTS. IT IS TO BE NOTED THAT A KIRBY-BAUER OR E-TEST WAS PERFORM ON THE CARBAPENEMS THAT HAD BEEN INTERMEDIATE OR RESISTANT. THE USER ALSO STATED THAT EACH ISOLATE TESTED SENSITIVE TO IMIPENEM BY KIRBY BAUER OR E-TEST. NO HEALTH IMPACT OR CONSEQUENCE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
697618 PANEL PHOENIX NMIC-312 SYSTEM, TEST, AUTOMATED, ANTIMICROBIAL SUSCEPTIBILITY, SHORT INCUBATION LON BECTON DICKINSON & CO. (SPARKS) 5324466 30382904490820

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown