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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device apparatus, suction, operating-room, wall vacuum powered
Regulation Description Vacuum-powered body fluid suction apparatus.
Product CodeGCX
Regulation Number 880.6740
Device Class 2

MDR Year MDR Reports MDR Events
2020 65 65
2021 65 65
2022 72 72
2023 59 59
2024 65 65
2025 196 196

Device Problems MDRs with this Device Problem Events in those MDRs
Smoking 60 60
Delivered as Unsterile Product 46 46
Break 40 40
Suction Failure 38 38
Temperature Problem 35 35
Leak/Splash 32 32
Suction Problem 32 32
Fluid/Blood Leak 28 28
Packaging Problem 27 27
Crack 25 25
Detachment of Device or Device Component 25 25
Overheating of Device 19 19
Material Fragmentation 17 17
Mechanical Problem 16 16
Contamination /Decontamination Problem 14 14
Obstruction of Flow 14 14
Device Contaminated During Manufacture or Shipping 14 14
Device Contamination with Chemical or Other Material 14 14
Contamination 13 13
Failure to Eject 12 12
Pressure Problem 9 9
Material Puncture/Hole 9 9
Decrease in Suction 8 8
Adverse Event Without Identified Device or Use Problem 8 8
Decrease in Pressure 7 7
Complete Blockage 7 7
Corroded 7 7
Noise, Audible 6 6
Fracture 4 4
Defective Device 4 4
Collapse 3 3
Insufficient Information 3 3
Material Separation 3 3
Defective Component 3 3
Sharp Edges 3 3
Excessive Heating 3 3
Nonstandard Device 3 3
Therapeutic or Diagnostic Output Failure 3 3
Self-Activation or Keying 3 3
No Flow 3 3
Shipping Damage or Problem 3 3
No Apparent Adverse Event 2 2
Device Emits Odor 2 2
Failure to Conduct 2 2
Power Problem 2 2
Continuous Firing 2 2
Use of Device Problem 2 2
Key or Button Unresponsive/not Working 2 2
Fumes or Vapors 2 2
Sparking 2 2

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 419 419
Insufficient Information 79 79
No Known Impact Or Consequence To Patient 20 20
Foreign Body In Patient 12 12
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 7 7
No Consequences Or Impact To Patient 7 7
Laceration(s) 5 5
Hemorrhage/Bleeding 4 4
Pneumothorax 3 3
No Patient Involvement 3 3
Pulmonary Edema 3 3
Device Embedded In Tissue or Plaque 3 3
Death 2 2
No Code Available 2 2
Cardiac Arrest 2 2
Exposure to Body Fluids 2 2
Hemothorax 2 2
Pleural Empyema 1 1
Deposits 1 1
Discomfort 1 1
Ulcer 1 1
Unspecified Heart Problem 1 1
Unspecified Respiratory Problem 1 1
Bacterial Infection 1 1
Low Blood Pressure/ Hypotension 1 1
Airway Obstruction 1 1
Liver Laceration(s) 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Cardinal Health 200, LLC II Jan-18-2024
2 Med Michigan Holding Llc II Dec-31-2024
3 Synaptive Medical Inc II Jun-25-2021
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