Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

New Search show TPLC since Back to Search Results
Device instruments, surgical, cardiovascular
Product CodeDWS
Regulation Number 870.4500
Device Class 1

MDR Year MDR Reports MDR Events
2017 40 40
2018 60 60
2019 28 28
2020 28 28
2021 32 32
2022 35 35
2023 18 18
2024 38 38

Device Problems MDRs with this Device Problem Events in those MDRs
Break 67 67
Mechanical Jam 34 34
Corroded 22 22
Failure to Cut 16 16
Physical Resistance/Sticking 15 15
Mechanical Problem 13 13
Difficult to Open or Close 13 13
Misfire 11 11
Detachment of Device or Device Component 11 11
Adverse Event Without Identified Device or Use Problem 11 11
Material Fragmentation 7 7
Contamination /Decontamination Problem 6 6
Entrapment of Device 6 6
Insufficient Information 6 6
Material Separation 6 6
Delivered as Unsterile Product 6 6
Fracture 6 6
Difficult to Remove 5 5
Device Operates Differently Than Expected 5 5
Component Missing 4 4
Detachment Of Device Component 4 4
Improper or Incorrect Procedure or Method 3 3
Packaging Problem 3 3
Activation, Positioning or Separation Problem 3 3
Sticking 2 2
No Apparent Adverse Event 2 2
Material Integrity Problem 2 2
Leak/Splash 2 2
Material Too Rigid or Stiff 2 2
Loose or Intermittent Connection 1 1
Failure to Disconnect 1 1
Noise, Audible 1 1
Dull, Blunt 1 1
Pitted 1 1
Out-Of-Box Failure 1 1
Structural Problem 1 1
Material Perforation 1 1
Mechanics Altered 1 1
Material Deformation 1 1
Device Fell 1 1
Material Erosion 1 1
Separation Failure 1 1
Material Disintegration 1 1
Device Markings/Labelling Problem 1 1
Failure to Eject 1 1
Positioning Problem 1 1
Manufacturing, Packaging or Shipping Problem 1 1
Crack 1 1
Physical Property Issue 1 1
Scratched Material 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 88 88
No Consequences Or Impact To Patient 65 65
No Known Impact Or Consequence To Patient 31 31
No Patient Involvement 29 29
Insufficient Information 18 18
No Information 14 14
Tissue Damage 14 14
Foreign Body In Patient 11 11
Not Applicable 4 4
Laceration(s) 4 4
Unspecified Tissue Injury 4 4
Device Embedded In Tissue or Plaque 4 4
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 3 3
Vascular Dissection 3 3
Perforation of Vessels 3 4
Cardiac Perforation 2 2
Death 1 1
Perforation 1 1
Blood Loss 1 1
Cardiac Tamponade 1 1
Unspecified Vascular Problem 1 1
Low Blood Pressure/ Hypotension 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Cook Vandergrift, Inc. II Sep-01-2023
2 Deroyal Industries, Inc. Lafollette II Feb-19-2020
3 Genesee BioMedical, Inc. II May-29-2018
4 Maquet Cardiovascular, LLC II Jul-31-2023
5 Maquet Cardiovascular, LLC II Apr-12-2022
6 TELEFLEX MEDICAL INC II Jan-27-2020
-
-