• 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 apparatus, suction, single patient use, portable, nonpowered
Regulation Description Nonpowered, single patient, portable suction apparatus.
Product CodeGCY
Regulation Number 878.4680
Device Class 1

MDR Year MDR Reports MDR Events
2021 216 217
2022 96 98
2023 90 91
2024 74 74
2025 182 182
2026 65 65

Device Problems MDRs with this Device Problem Events in those MDRs
Disconnection 140 140
Device Contamination with Chemical or Other Material 76 76
Suction Failure 73 73
Material Fragmentation 62 62
Dull, Blunt 50 50
Fluid/Blood Leak 34 35
Break 29 29
Material Split, Cut or Torn 25 26
Decrease in Suction 17 18
Nonstandard Device 11 11
Fracture 11 12
Component Misassembled 10 10
Component Missing 9 9
Fitting Problem 9 9
Inflation Problem 9 9
Partial Blockage 8 8
Insufficient Device Problem Information 8 8
Suction Problem 7 7
Tear, Rip or Hole in Device Packaging 6 6
Detachment of Device or Device Component 6 6
Device Contaminated During Manufacture or Shipping 6 6
Crack 6 6
Incorrect Measurement 5 5
Defective Device 5 5
Unsealed Device Packaging 4 4
Restricted Flow rate 4 4
Complete Blockage 4 4
Material Twisted/Bent 4 4
No Apparent Adverse Event 4 4
Material Too Soft/Flexible 4 4
Incomplete or Missing Packaging 3 3
Burst Container or Vessel 3 3
Patient Device Interaction Problem 2 2
Scratched Material 2 2
Adverse Event Without Identified Device or Use Problem 2 2
Collapse 2 2
Device Dislodged or Dislocated 2 2
Deformation Due to Compressive Stress 2 2
Inadequate Instructions for Healthcare Professional 2 2
Use of Device Problem 2 2
Material Separation 2 2
Device Damaged Prior to Use 2 2
Difficult to Remove 2 2
Obstruction of Flow 2 2
Leak/Splash 2 2
Physical Resistance/Sticking 1 1
Sharp Edges 1 1
Output Problem 1 1
Material Protrusion/Extrusion 1 1
Material Integrity Problem 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 580 582
Foreign Body In Patient 57 57
No Consequences Or Impact To Patient 29 29
Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available 27 29
Insufficient Information 26 26
Exposure to Body Fluids 23 23
Hematoma 12 13
Unspecified Infection 9 9
Post Operative Wound Infection 8 8
Device Embedded In Tissue or Plaque 7 7
No Patient Involvement 5 5
Pain 3 3
Laceration(s) 2 2
Bacterial Infection 2 2
Granuloma 2 2
Inflammation 1 1
Hypersensitivity/Allergic reaction 1 1
Anemia 1 1
Wound Dehiscence 1 1
No Code Available 1 1
Hemorrhage/Blood Loss/Bleeding 1 1
Impaired Healing 1 1
Purulent Discharge 1 1
Unspecified Tissue Injury 1 1
Fluid Discharge 1 1
Muscle Weakness/Atrophy 1 1
Abscess 1 1
Cellulitis 1 1
Seroma 1 1
Tissue Breakdown 1 1
Pneumothorax 1 1
Sepsis 1 1
Joint Laxity 1 1
Pressure Sore/Ulcer 1 1
Skin Inflammation/ Irritation 1 1
Discomfort 1 1
Swelling/ Edema 1 1
Injury 1 1
Colitis 1 1

-
-