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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device tubing, noninvasive
Regulation Description Vacuum-powered body fluid suction apparatus.
Product CodeGAZ
Regulation Number 880.6740
Device Class 2

MDR Year MDR Reports MDR Events
2021 18 18
2022 12 12
2023 24 25
2024 65 65
2025 42 42
2026 51 51

Device Problems MDRs with this Device Problem Events in those MDRs
Defective Device 79 79
Detachment of Device or Device Component 34 35
Suction Failure 10 10
Defective Component 9 9
Fitting Problem 8 8
Suction Problem 7 7
Material Twisted/Bent 4 4
Disconnection 3 3
Leak/Splash 3 3
No Flow 3 3
Complete Blockage 3 3
Obstruction of Flow 3 3
Gas/Air Leak 3 3
Failure to Cut 3 3
Loose or Intermittent Connection 2 2
Break 2 2
Key or Button Unresponsive/not Working 2 2
Product Quality Problem 2 2
Backflow 2 2
Material Rupture 2 2
Decrease in Suction 2 2
Radiofrequency Interference (RFI) 1 1
Connection Problem 1 1
Failure to Advance 1 1
Failure to Conduct 1 1
Appropriate Device Problem Term/Code Not Available 1 1
Material Separation 1 1
Failure to Prime 1 1
Insufficient Flow or Under Infusion 1 1
Improper Flow or Infusion 1 1
Component Missing 1 1
Use of Device Problem 1 1
No Pressure 1 1
Ejection Problem 1 1
Contamination /Decontamination Problem 1 1
Difficult to Remove 1 1
Positioning Problem 1 1
Inability to Irrigate 1 1
Filling Problem 1 1
Mechanical Problem 1 1
Separation Problem 1 1
Material Split, Cut or Torn 1 1
Pressure Problem 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 178 179
Insufficient Information 31 31
Intraocular Pressure Increased 1 1
Endophthalmitis 1 1
Bradycardia 1 1
Vitreous Hemorrhage 1 1
Hypoxia 1 1
Retinal Tear 1 1

Recalls
Manufacturer Recall Class Date Posted
1 DeRoyal Industries Inc II Mar-05-2025
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