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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle
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Device heparin, vascular access flush
Definition Enhance the performance of intravascular catheters, to maintain patency of the vascular catheter when it is not in use.
Product CodeNZW
Regulation Number 880.5200
Device Class 2


Premarket Reviews
ManufacturerDecision
APP PHARMACEUTICALS, LLC
  SUBSTANTIALLY EQUIVALENT 1
BECTON DICKINSON & CO.
  SUBSTANTIALLY EQUIVALENT 1
BECTON DICKINSON AND COMPANY
  SUBSTANTIALLY EQUIVALENT 1
EXCELSIOR MEDICAL CORPORATION
  SUBSTANTIALLY EQUIVALENT 1
MEDEFIL, INC.
  SUBSTANTIALLY EQUIVALENT 1

MDR Year MDR Reports MDR Events
2014 8 8
2015 5 5
2017 3 3
2018 19 19
2019 19 19
2020 2 2
2021 10 10
2022 14 14
2023 9 9
2024 6 6

Device Problems MDRs with this Device Problem Events in those MDRs
Device Markings/Labelling Problem 23 23
Nonstandard Device 9 9
Manufacturing, Packaging or Shipping Problem 8 8
Adverse Event Without Identified Device or Use Problem 8 8
Packaging Problem 5 5
Leak/Splash 4 4
Patient-Device Incompatibility 4 4
Insufficient Information 4 4
Device Contamination with Chemical or Other Material 4 4
Microbial Contamination of Device 4 4
Device Operates Differently Than Expected 4 4
Missing Information 3 3
Crack 2 2
Lack of Effect 2 2
Break 2 2
Volume Accuracy Problem 2 2
Off-Label Use 2 2
Disconnection 1 1
Device Damaged Prior to Use 1 1
Short Fill 1 1
Sediment, Precipitate Or Deposit In Device Or Device Ingredient 1 1
Defective Component 1 1
Defective Device 1 1
Labelling, Instructions for Use or Training Problem 1 1
Fluid/Blood Leak 1 1
Hole In Material 1 1
Contamination /Decontamination Problem 1 1
Failure to Deliver 1 1
Shipping Damage or Problem 1 1
Delivered as Unsterile Product 1 1
Appropriate Term/Code Not Available 1 1
Protective Measures Problem 1 1
Flushing Problem 1 1
Incorrect Device Or Component Shipped 1 1
Unintended Ejection 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Known Impact Or Consequence To Patient 22 22
No Clinical Signs, Symptoms or Conditions 20 20
Insufficient Information 10 10
No Patient Involvement 6 6
Fever 5 5
Bacterial Infection 5 5
Unspecified Infection 4 4
Nausea 4 4
Death 3 3
Sepsis 3 3
Reaction 3 3
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 2 2
Sweating 2 2
Respiratory Distress 2 2
Seizures 2 2
No Information 2 2
Chemical Exposure 2 2
Diarrhea 2 2
Septic Shock 2 2
Hemorrhage/Bleeding 2 2
No Consequences Or Impact To Patient 2 2
Abdominal Pain 1 1
Hypersensitivity/Allergic reaction 1 1
Complaint, Ill-Defined 1 1
Dizziness 1 1
Inflammation 1 1
Malaise 1 1
Taste Disorder 1 1
Cardiac Arrest 1 1
Staphylococcus Aureus 1 1
Alteration In Body Temperature 1 1
Chills 1 1
Foreign Body In Patient 1 1
Swelling 1 1
Thrombosis 1 1
Vomiting 1 1
Numbness 1 1
Pain 1 1
Constipation 1 1
Low Blood Pressure/ Hypotension 1 1

Recalls
Manufacturer Recall Class Date Posted
1 App Pharmaceuticals Llc II Jun-19-2012
2 Excelsior Medical Corp II Jun-14-2016
3 Excelsior Medical Corp II Jun-05-2012
4 Fresenius Kabi USA, LLC II Jan-29-2015
5 Mckesson Medical-Surgical Inc. Corporate Office II Aug-26-2022
6 Medefil Incorporated III Mar-06-2014
7 Medefil Incorporated II Dec-10-2010
8 Vygon Corporation II Jun-13-2012
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