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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle
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Device adaptor, stopcock, manifold, fitting, cardiopulmonary bypass
Regulation Description Cardiopulmonary bypass adaptor, stopcock, manifold, or fitting.
Product CodeDTL
Regulation Number 870.4290
Device Class 2

MDR Year MDR Reports MDR Events
2019 76 76
2020 53 53
2021 55 55
2022 48 48
2023 46 46
2024 453 453
2025 21 21

Device Problems MDRs with this Device Problem Events in those MDRs
Leak/Splash 368 368
Human-Device Interface Problem 123 123
Loose or Intermittent Connection 85 85
Air/Gas in Device 57 57
Fluid/Blood Leak 28 28
Physical Resistance/Sticking 21 21
Improper or Incorrect Procedure or Method 19 19
Display or Visual Feedback Problem 17 17
Defective Device 8 8
Fitting Problem 7 7
Material Deformation 7 7
Gas/Air Leak 7 7
Inflation Problem 6 6
Failure to Cycle 6 6
Break 6 6
Tear, Rip or Hole in Device Packaging 5 5
Device-Device Incompatibility 5 5
Difficult to Advance 5 5
Adverse Event Without Identified Device or Use Problem 5 5
Device Contamination with Chemical or Other Material 4 4
Contamination /Decontamination Problem 4 4
Product Quality Problem 4 4
Crack 4 4
Deflation Problem 3 3
Difficult to Insert 3 3
Unsealed Device Packaging 3 3
Difficult to Remove 3 3
Unstable 3 3
Therapeutic or Diagnostic Output Failure 3 3
No Apparent Adverse Event 3 3
Noise, Audible 2 2
Detachment of Device or Device Component 2 2
Material Split, Cut or Torn 2 2
Material Separation 2 2
Device Difficult to Setup or Prepare 2 2
Material Puncture/Hole 2 2
Fracture 2 2
Mechanical Problem 2 2
Contamination 2 2
Corroded 1 1
Backflow 1 1
Flushing Problem 1 1
Delivered as Unsterile Product 1 1
Unable to Obtain Readings 1 1
Device Slipped 1 1
Incorrect, Inadequate or Imprecise Result or Readings 1 1
Use of Device Problem 1 1
Device Contamination with Body Fluid 1 1
Connection Problem 1 1
Separation Failure 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 585 585
No Consequences Or Impact To Patient 60 60
Blood Loss 42 42
Air Embolism 19 19
Insufficient Information 17 17
No Known Impact Or Consequence To Patient 14 14
Hemorrhage/Bleeding 10 10
No Patient Involvement 6 6
No Information 5 5
Injury 5 5
Low Blood Pressure/ Hypotension 3 3
Ventricular Fibrillation 3 3
Non specific EKG/ECG Changes 2 2
Death 1 1
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 1 1
Overdose 1 1
Not Applicable 1 1
Arrhythmia 1 1
Myocardial Infarction 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Boston Scientific Corporation II May-16-2023
2 LivaNova USA Inc. III Jul-17-2020
3 LivaNova USA Inc. II Jun-26-2020
4 MEDLINE INDUSTRIES, LP - Northfield II Sep-06-2024
5 Medline Industries Inc II Sep-24-2021
6 Merit Medical Systems, Inc. II Apr-11-2022
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