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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device flow cytometric reagents and accessories.
Definition To identify and classify cells or other particles in suspension by their inherent physical properties or associated fluorescent molecules in order to provide information about the distribution or number cells in suspension or their level of protein expression. These characteristics may aid in the diagnosis of conditions such as immunodeficiency and cancer.
Product CodeOYE
Regulation Number 864.5220
Device Class 2


Premarket Reviews
ManufacturerDecision
BD BIOSCIENCES
  SUBSTANTIALLY EQUIVALENT 2
BECKMAN COULTER
  SUBSTANTIALLY EQUIVALENT 1
BECKMAN COULTER, INC
  SUBSTANTIALLY EQUIVALENT 1
BECKMAN COULTER, INC.
  SUBSTANTIALLY EQUIVALENT 4
BECTON, DICKINSON & COMPANY
  SUBSTANTIALLY EQUIVALENT 2
BECTON, DICKINSON AND COMPANY
  SUBSTANTIALLY EQUIVALENT 2

MDR Year MDR Reports MDR Events
2014 9 9
2015 6 6
2016 2 2
2017 9 9
2018 25 25
2019 6 6
2020 173 173
2021 251 251
2022 193 193
2023 142 142
2024 17 17

Device Problems MDRs with this Device Problem Events in those MDRs
Fluid/Blood Leak 357 357
Incorrect, Inadequate or Imprecise Result or Readings 266 266
Contamination 100 100
Leak/Splash 31 31
Device Operational Issue 30 30
Improper or Incorrect Procedure or Method 10 10
Device Markings/Labelling Problem 6 6
Device Operates Differently Than Expected 6 6
Break 5 5
Device Contamination with Chemical or Other Material 4 4
Data Problem 4 4
Use of Device Problem 3 3
Adverse Event Without Identified Device or Use Problem 3 3
Output Problem 3 3
Pressure Problem 2 2
Unable to Obtain Readings 2 2
Device Inoperable 2 2
Contamination of Device Ingredient or Reagent 2 2
Signal Artifact/Noise 2 2
Computer Software Problem 2 2
Patient Data Problem 2 2
Non Reproducible Results 2 2
Thermal Decomposition of Device 1 1
Charred 1 1
Application Program Problem: Dose Calculation Error 1 1
Electrical /Electronic Property Problem 1 1
False Positive Result 1 1
Fire 1 1
Loose or Intermittent Connection 1 1
Mechanical Problem 1 1
Device Emits Odor 1 1
Inadequate or Insufficient Training 1 1
Flushing Problem 1 1
Device Ingredient or Reagent Problem 1 1
Defective Component 1 1
Device Contamination with Body Fluid 1 1
Device Displays Incorrect Message 1 1
Protective Measures Problem 1 1
Electrical Power Problem 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 633 633
No Consequences Or Impact To Patient 114 114
No Patient Involvement 85 85
Test Result 33 33
No Known Impact Or Consequence To Patient 17 17
Not Applicable 6 6
Electric Shock 2 2
Chemical Exposure 2 2
Superficial (First Degree) Burn 1 1
Injury 1 1
Numbness 1 1
Eye Injury 1 1
Tingling 1 1
No Information 1 1

Recalls
Manufacturer Recall Class Date Posted
1 BD Biosciences, Systems & Reagents II Jun-26-2015
2 BD Biosciences, Systems & Reagents II Jul-02-2014
3 Beckman Coulter Inc. II Oct-11-2018
4 Beckman Coulter Inc. II Apr-10-2018
5 Beckman Coulter Inc. II Sep-19-2017
6 Beckman Coulter Inc. II Apr-17-2017
7 Beckman Coulter Inc. II Nov-21-2016
8 Beckman Coulter Inc. II Sep-28-2016
9 Becton, Dickinson and Company, BD Biosciences II Oct-09-2019
10 Becton, Dickinson and Company, BD Biosciences III Feb-01-2019
11 Becton, Dickinson and Company, BD Biosciences III Jul-13-2018
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