MAUDE Adverse Event Report: BECTON, DICKINSON & CO. (SPARKS) BD PHOENIX M50 AUTOMATED MICROBIOLOGY SYSTEM; SYSTEM, TEST, AUTOMATED ANTIMICROBIAL SUSCEPTIBILITY, SHORT INCUBATION

Model Number	448105
Medical Device Problem Code	Incorrect, Inadequate or Imprecise Result or Readings (1535)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	03/03/2021
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
A device evaluation and/or device history review is anticipated, but is not complete.Upon completion, a supplemental report will be filed.
Event or Problem Description
It was reported that while using bd (b)(6) m50 automated microbiology system incorrect data was reported to the laboratory personnel by the instrument.There was no indication that incorrect results were reported out and there was no report of patient impact.
Event or Problem Description
It was reported that while using bd phoenix¿ m50 automated microbiology system incorrect data was reported to the laboratory personnel by the instrument.There was no indication that incorrect results were reported out and there was no report of patient impact.
Additional Manufacturer Narrative
It was determined in review of this record that the incorrect guideline was used to complete the decision tree for this product.A new not reportable decision tree has been completed using the phoenix guidelines instead.After review it was determined to be a ups failure.This mdr should be considered cancelled.

• Brand Name: BD PHOENIX M50 AUTOMATED MICROBIOLOGY SYSTEM
• Common Device Name: SYSTEM, TEST, AUTOMATED ANTIMICROBIAL SUSCEPTIBILITY, SHORT INCUBATION
• Manufacturer (Section D): BECTON, DICKINSON & CO. (SPARKS); 7 loveton circle; sparks MD 21152
• MDR Report Key: 11568739
• Report Number: 1119779-2021-00557
• Device Sequence Number: 4266776
• Product Code: LON
• UDI-Device Identifier: 00382904481056
• UDI-Public: 00382904481056
• Combination Product (Y/N): N
• Initial Reporter Country: FR
• PMA/510(K) Number: K020321
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: foreign,other,user facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 04/05/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Other
• Device Model Number: 448105
• Device Catalogue Number: 448105
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 03/03/2021
• Supplement Date Received by Manufacturer: 03/03/2021
• Initial Report FDA Received Date: 03/25/2021
• Supplement Report FDA Received Date: 04/05/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1