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TPLC
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Device
tube, double lumen for intestinal decompression and/or intubation
Regulation Description
Gastrointestinal tube and accessories.
Product Code
FEG
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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