FDA Adverse Event Malfunction Summary report: N

BD PHOENIX¿ NMIC-306

MDR report key: 23404742 · Received October 28, 2025

Report

Report Number
1119779-2025-05174
Event Type
Malfunction
Date Received
October 28, 2025
Date of Event
September 29, 2025
Report Date
February 2, 2026
Manufacturer
BECTON DICKINSON & CO. (SPARKS)
Product Code
LON
UDI-DI
30382904492923
PMA / PMN Number
SEE H11
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

E1. INITIAL REPORTER PHONE #: (B)(6). THERE WERE MULTIPLE 510K NUMBERS REPORTED TO BE INVOLVED. THE INFORMATION FOR THE ADDITIONAL 510K IS AS FOLLOWS: G4. PMA / 510(K)#: K020322, K022129, K023444, K023634, K023858, K024153, 031530, K031699, K031912, K032299, K032567, K032655, K032675, K033362, K033458, K033558, K033560, K041384, K042932, K052269, K060214, 060217, K060257, K060444, K060447, K061327, K061355, K061867, K062207, K062944, K063301, AND K06348. H3. A DEVICE EVALUATION IS ANTICIPATED BUT HAS NOT YET BEGUN. UPON COMPLETION OF THE INVESTIGATION, A SUPPLEMENTAL REPORT WILL BE FILED.

Additional Manufacturer Narrative · 0

INVESTIGATION SUMMARY: THIS COMPLAINT IS FOR HIGH MIC ERTAPENEM (ETP) WHEN USING PANEL PHOENIX NMIC-306 (CATALOG NUMBER 449292) BATCH NUMBER 5196167. THE CUSTOMER RETURNED BINARY FILES, ISOLATES AND PHOENIX GENERATED LAB REPORTS FOR THE INVESTIGATION. THE BATCH HISTORY RECORD WAS SATISFACTORY, AND NO QUALITY NOTIFICATIONS WERE GENERATED DURING MANUFACTURING AND INSPECTION. TO INVESTIGATE, RETENTION PANELS FROM THE COMPLAINT BATCH WERE INOCULATED WITH CUSTOMER RETURNED ISOLATES ENTEROBACTER CLOACAE COMPLEX 337343312 AND KLEBSIELLA PNEUMONIAE 3771419 TO OBSERVE FOR ETP MIC RESULTS. NEXT, CONTROL PANELS FROM THE SAME MATERIAL BUT DIFFERENT BATCH WERE INOCULATED WITH CUSTOMER RETURNED ISOLATES ENTEROBACTER CLOACAE COMPLEX 337343312 AND KLEBSIELLA PNEUMONIAE 3771419 TO OBSERVE FOR ETP MIC RESULTS. THE INVESTIGATION RETURNED ALL PANELS WITH INTERMEDIATE AND RESISTANT ETP MIC RESULTS. FOR FURTHER INVESTIGATION, DISK DIFFUSION WAS PERFORMED ON CUSTOMER RETURNED ISOLATES ENTEROBACTER CLOACAE COMPLEX 337343312 AND KLEBSIELLA PNEUMONIAE 3771419. THE DISK DIFFUSION RESULTS SHOW BOTH ISOLATES WITH RESISTANCE TO ETP. AS ALL PANELS TESTED WERE EITHER INTERMEDIATE OR RESISTANT ETP MIC RESULTS, THIS COMPLAINT IS UNABLE TO BE CONFIRMED. BD DOES NOT CONFIRM ON AN INTERMEDIATE (I) RESULT, AS IT IS ONE DILUTION OFF FROM SENSITIVE (S) OR RESISTANT (R). COMPLAINT TRENDING WAS PERFORMED, AND NO TRENDS WERE IDENTIFIED ASSOCIATED WITH THIS DEFECT. AS NO TRENDS WERE IDENTIFIED, NO CORRECTIVE ACTIONS ARE SLATED AT THIS TIME. BD WILL CONTINUE TO MONITOR FOR TRENDS AND TAKE ACTION AS NECESSARY. PLEASE CONTINUE TO COMMUNICATE ANY ADDITIONAL CONCERNS.

Description of Event or Problem · 0

IT WAS REPORTED WHILE USING THE BD PHOENIX¿ NMIC-306 A PATIENT ISOLATE HAD HIGH MICS (FALSE RESISTANT RESULT) FOR THE DRUG ERTAPENEM. THE USER NOTED USING AN E-TEST STRIP FOR CONFIRMATORY TESTING GIVING A SUSCEPTIBLE RESULT. NO HEALTH IMPACT OR CONSEQUENCE REPORTED.

Description of Event or Problem · 0

IT WAS REPORTED WHILE USING THE BD PHOENIX¿ NMIC-306 A PATIENT ISOLATE HAD HIGH MICS (FALSE RESISTANT RESULT) FOR THE DRUG ERTAPENEM. THE USER NOTED USING AN E-TEST STRIP FOR CONFIRMATORY TESTING GIVING A SUSCEPTIBLE RESULT. NO HEALTH IMPACT OR CONSEQUENCE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
112695 BD PHOENIX¿ NMIC-306 SYSTEM, TEST, AUTOMATED, ANTIMICROBIAL SUSCEPTIBILITY, SHORT INCUBATION LON BECTON DICKINSON & CO. (SPARKS) 5196167 30382904492923

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown