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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device tube, double lumen for intestinal decompression and/or intubation
Regulation Description Gastrointestinal tube and accessories.
Product CodeFEG
Regulation Number 876.5980
Device Class 2

MDR Year MDR Reports MDR Events
2021 27 27
2022 40 40
2023 33 33
2024 31 31
2025 46 46
2026 16 16

Device Problems MDRs with this Device Problem Events in those MDRs
Break 25 25
Fluid/Blood Leak 15 15
Off-Label Use 14 14
Material Split, Cut or Torn 12 12
Insufficient Device Problem Information 10 10
Difficult to Remove 9 9
Separation Failure 8 8
Partial Blockage 8 8
Defective Component 7 7
Unclear Information 7 7
Component Missing 6 6
Device Contamination with Chemical or Other Material 6 6
Component Misassembled 6 6
Suction Failure 5 5
Crack 5 5
Adverse Event Without Identified Device or Use Problem 5 5
Material Too Soft/Flexible 5 5
Material Fragmentation 4 4
Material Too Rigid or Stiff 3 3
Nonstandard Device 3 3
Incorrect Measurement 3 3
Loose or Intermittent Connection 2 2
Leak/Splash 2 2
Fracture 2 2
Physical Resistance/Sticking 2 2
Material Twisted/Bent 2 2
Biocompatibility 2 2
Inaccurate Information 2 2
Separation Problem 2 2
Defective Device 2 2
Fitting Problem 2 2
Suction Problem 2 2
Migration 1 1
Patient Device Interaction Problem 1 1
No Apparent Adverse Event 1 1
Difficult to Open or Close 1 1
Detachment of Device or Device Component 1 1
Decrease in Suction 1 1
Positioning Failure 1 1
Disconnection 1 1
Deformation Due to Compressive Stress 1 1
Malposition of Device 1 1
Dent in Material 1 1
Improper or Incorrect Procedure or Method 1 1
Material Separation 1 1
Increase in Suction 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 150 150
Insufficient Information 11 11
Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available 9 9
Foreign Body In Patient 4 4
Discomfort 3 3
Aspiration/Inhalation 3 3
Hemorrhage/Blood Loss/Bleeding 3 3
Anxiety 2 2
Perforation 2 2
Perforation of Esophagus 2 2
Hematoma 2 2
Pain 2 2
Pneumothorax 2 2
Vomiting 2 2
Nausea 1 1
Gastrointestinal Regurgitation 1 1
Exposure to Body Fluids 1 1
Pressure Sore/Ulcer 1 1
Septic Shock 1 1
Low Blood Pressure/ Hypotension 1 1
No Consequences Or Impact To Patient 1 1
Pneumonia 1 1
Internal Organ Perforation 1 1
Swelling/ Edema 1 1
Tachycardia 1 1
Unspecified Gastrointestinal Problem 1 1
Epistaxis 1 1
Fever 1 1
Feeding Problem 1 1

Recalls
Manufacturer Recall Class Date Posted
1 C.R. Bard Inc II Jan-25-2024
2 Cardinal Health 200, LLC II Oct-17-2025
3 Cardinal Health 200, LLC II Sep-26-2024
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