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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle
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Device infusor, pressure, for i.v. bags
Product CodeKZD
Regulation Number 880.5420
Device Class 1

MDR Year MDR Reports MDR Events
2019 4 4
2020 8 8
2021 13 13
2022 45 45
2023 31 31
2024 9 9

Device Problems MDRs with this Device Problem Events in those MDRs
Leak/Splash 28 28
Gas/Air Leak 16 16
Pressure Problem 15 15
Unintended Deflation 6 6
Material Integrity Problem 4 4
Mechanical Problem 4 4
Decrease in Pressure 4 4
Disconnection 4 4
Break 3 3
Burst Container or Vessel 3 3
Crack 3 3
Defective Device 3 3
Detachment of Device or Device Component 2 2
Inflation Problem 2 2
Device Handling Problem 2 2
Fluid/Blood Leak 2 2
Fracture 2 2
Incorrect, Inadequate or Imprecise Result or Readings 2 2
Use of Device Problem 1 1
Failure to Zero 1 1
Insufficient Flow or Under Infusion 1 1
Component Missing 1 1
Inaccurate Delivery 1 1
Obstruction of Flow 1 1
Material Fragmentation 1 1
No Display/Image 1 1
Deflation Problem 1 1
Contamination 1 1
Explosion 1 1
Material Split, Cut or Torn 1 1
Incomplete or Inadequate Connection 1 1
Failure to Deflate 1 1
Air/Gas in Device 1 1
Backflow 1 1
Free or Unrestricted Flow 1 1
Insufficient Information 1 1
Appropriate Term/Code Not Available 1 1
Inadequate User Interface 1 1
Infusion or Flow Problem 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 69 69
Insufficient Information 25 25
Air Embolism 3 3
No Known Impact Or Consequence To Patient 3 3
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 2 2
Urinary Tract Infection 2 2
No Patient Involvement 1 1
Foreign Body In Patient 1 1
Not Applicable 1 1
Embolism/Embolus 1 1
Respiratory Arrest 1 1
Respiratory Insufficiency 1 1
Arrhythmia 1 1
Atrial Fibrillation 1 1
Cardiac Arrest 1 1
Hearing Impairment 1 1

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