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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device syringe, balloon inflation
Regulation Description Angiographic injector and syringe.
Product CodeMAV
Regulation Number 870.1650
Device Class 2


Premarket Reviews
ManufacturerDecision
MEDTRONIC VASCULAR
  SUBSTANTIALLY EQUIVALENT 1

MDR Year MDR Reports MDR Events
2020 101 101
2021 186 186
2022 437 437
2023 220 222
2024 420 421
2025 66 66
2026 2 2

Device Problems MDRs with this Device Problem Events in those MDRs
Leak/Splash 978 978
Loose or Intermittent Connection 202 202
Display or Visual Feedback Problem 157 159
Break 84 84
Physical Resistance/Sticking 46 46
Incorrect, Inadequate or Imprecise Result or Readings 46 46
Device Contamination with Chemical or Other Material 44 44
Inflation Problem 28 28
Unsealed Device Packaging 24 24
Packaging Problem 19 19
Material Separation 16 16
Deflation Problem 12 12
Improper or Incorrect Procedure or Method 12 12
Contamination 11 11
Tear, Rip or Hole in Device Packaging 11 11
Material Integrity Problem 8 8
Appropriate Term/Code Not Available 8 8
Defective Device 7 7
Adverse Event Without Identified Device or Use Problem 6 6
Noise, Audible 6 6
Shipping Damage or Problem 6 6
Device Contaminated During Manufacture or Shipping 5 5
Mechanical Problem 5 5
Product Quality Problem 5 5
Crack 4 4
Detachment of Device or Device Component 4 4
Failure to Zero 4 4
Fluid/Blood Leak 3 3
Difficult to Open or Remove Packaging Material 3 3
Obstruction of Flow 3 3
Unstable 3 3
Device Sensing Problem 2 2
Connection Problem 2 2
Contamination /Decontamination Problem 2 2
Material Rupture 2 2
Difficult to Remove 2 2
Insufficient Information 2 2
Pressure Problem 2 2
Output Problem 2 2
Mechanical Jam 2 2
Use of Device Problem 1 1
Retraction Problem 1 1
Suction Problem 1 1
Device Damaged Prior to Use 1 1
Defective Component 1 1
Moisture Damage 1 1
Material Split, Cut or Torn 1 1
Low Readings 1 1
Deformation Due to Compressive Stress 1 1
Unintended Movement 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 1300 1302
No Consequences Or Impact To Patient 90 90
Insufficient Information 17 17
Air Embolism 6 6
No Patient Involvement 6 6
No Known Impact Or Consequence To Patient 5 5
Arrhythmia 3 3
Vascular Dissection 3 3
Cardiac Arrest 3 3
Laceration(s) 3 3
Low Blood Pressure/ Hypotension 3 3
Hemorrhage/Bleeding 2 2
Perforation 1 1
Ventricular Fibrillation 1 1
Thrombosis/Thrombus 1 1
Bradycardia 1 1
Perforation of Vessels 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Abbott Vascular II Apr-13-2022
2 Abbott Vascular Inc II Dec-20-2024
3 Boston Scientific Corporation II Sep-05-2025
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