FDA Adverse Event Malfunction Summary report: N

BD BBL¿ MUELLER HINTON II AGAR 150MM PLATE 24PK

MDR report key: 15552419 · Received October 6, 2022

Report

Report Number
1119779-2022-01279
Event Type
Malfunction
Date Received
October 6, 2022
Date of Event
September 29, 2022
Report Date
February 8, 2023
Manufacturer
BECTON, DICKINSON & CO. (SPARKS)
Product Code
JTZ
UDI-DI
10382902218002
PMA / PMN Number
PREAMENDMENT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

A DEVICE EVALUATION AND/OR DEVICE HISTORY REVIEW IS ANTICIPATED BUT IS NOT COMPLETE. UPON COMPLETION, A SUPPLEMENTAL REPORT WILL BE FILED.

Additional Manufacturer Narrative · 0

DURING MANUFACTURING OF MATERIAL 221800, MEDIA IS FORMULATED AND SENT THROUGH A HIGH TEMPERATURE SHORT TIME STERILIZER TO REMOVE BIOBURDEN. THE PETRI DISHES ARE SUBJECTED TO UV RADIATION TO DECREASE BIOBURDEN. THE PETRI DISHES ARE FILLED IN A POSITIVE PRESSURE HEPA FILTERED ENVIRONMENT. THE FILLED PLATES ARE COOLED AND IMMEDIATELY WRAPPED INTO SLEEVES TO DECREASE THE INTRODUCTION OF MICROBES. SLEEVES ARE THEN PACKAGED INTO CARTONS AND THEN TRANSFERRED TO A REFRIGERATED TRUCK 2 TO 8 DEGREES CELSIUS (C) FOR SHIPMENT TO THE DISTRIBUTOR. BD DISTRIBUTORS ARE PROVIDED WITH THE STORAGE GUIDELINES FOR THE SHIPPING AND HANDLING OF BD MEDIA OF 2 TO 8 DEGREES C IN A DARK PLACE. THE BATCH HISTORY RECORD REVIEW FOR BATCH 2242624 WAS SATISFACTORY PER INTERNAL PROCEDURES. THE RELEASE TESTING THAT IS PERFORMED ON THIS PRODUCT DOES INCLUDE BIOBURDEN TESTING. A SAMPLE OF PLATES ARE INCUBATED AT 25 DEGREES C AND AT 35 DEGREES C FOR APPROXIMATELY 72 HOURS. ALL BIOBURDEN TESTING PERFORMED ON THIS BATCH WAS SATISFACTORY PER BD INTERNAL PROCEDURES. AFFECTED PRODUCT DOES NOT HAVE ANY STERILITY CLAIMS; THE PRODUCT IS TESTED FOR BIOBURDEN PRIOR TO RELEASE TO ENSURE THAT IT CONFORMS TO PRODUCT SPECIFICATIONS. HOWEVER, THIS DOES NOT ENSURE THAT THE END-USER WILL NOT RECEIVE A CONTAMINATED PLATE. THE COMPLAINT HISTORY WAS REVIEWED, AND NO OTHER COMPLAINTS HAVE BEEN TAKEN ON BATCH 2242624. NO RETENTION SAMPLES FOR THIS BATCH WERE AVAILABLE FOR INVESTIGATION. TWO PHOTOS WERE RECEIVED. PHOTO ONE SHOWS ONE PLATE (LOT ILLEGIBLE TIMESTAMP 1101) WITH A LARGE COLONY COVERING ALMOST HALF OF THE PLATE. PHOTO TWO SHOWS PART OF A SLEEVE OF PLATES WITH CONTAMINATION VISIBLE IN THE PLATES THROUGH THE SLEEVE, NO ID VISIBLE. BD HAS IDENTIFIED A CONTAMINATION TREND FOR THIS PRODUCT AND THE INVESTIGATION FOUND OPPORTUNITIES FOR BIOBURDEN REDUCTION IN THE MANUFACTURING PROCESS. A CAPA (CORRECTIVE AND PREVENTATIVE ACTIONS) HAS BEEN INITIATED AND INVOLVES IMPLEMENTING ADDITIONAL CLEANING EVENTS AND EVALUATION OF MANUFACTURING PROCEDURES FOCUSED ON IN-PROCESS BIOBURDEN REDUCTION. ADDITIONAL TRAININGS ARE PLANNED WITH AN ONGOING TRAINING REVIEW FOR CLEANING PROCESSES. IMPROVEMENT IN OBSERVATION OF CONTAMINATION IS EXPECTED AS THE CAPA PROGRESSES. H3 OTHER TEXT : SEE H.10.

Description of Event or Problem · 0

IT WAS REPORTED THAT BD BBL¿ MUELLER HINTON II AGAR HAS SEVEN OCCURRENCES OF CONTAMINATION. THE PRODUCT IS CLOUDY AND HAS CHANGED COLOR. THE MEDIA CONTAMINATION WAS NOTICED UPON RECEIVING. NO PATIENT IMPACT WAS REPORTED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CUSTOMER STATES MEDIA IS CONTAMINATED. PRODUCT IS CLOUDY AND HAS CHANGED COLOR.

Description of Event or Problem · 0

IT WAS REPORTED THAT BD BBL¿ MUELLER HINTON II AGAR HAS SEVEN OCCURRENCES OF CONTAMINATION. THE PRODUCT IS CLOUDY AND HAS CHANGED COLOR. THE MEDIA CONTAMINATION WAS NOTICED UPON RECEIVING. NO PATIENT IMPACT WAS REPORTED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CUSTOMER STATES MEDIA IS CONTAMINATED. PRODUCT IS CLOUDY AND HAS CHANGED COLOR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
275342 BD BBL¿ MUELLER HINTON II AGAR 150MM PLATE 24PK CULTURE MEDIA, ANTIMICROBIAL SUSCEPTIBILITY TEST, MUELLER HINTON AGAR/BROTH JTZ BECTON, DICKINSON & CO. (SPARKS) 221800 2242624 10382902218002

Patients

Seq Age Sex Outcome Treatment
1 Unknown