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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device catheter, conduction, anesthetic
Regulation Description Anesthesia conduction catheter.
Product CodeBSO
Regulation Number 868.5120
Device Class 2


Premarket Reviews
ManufacturerDecision
B. BRAUN MEDICAL, INC.
  SUBSTANTIALLY EQUIVALENT 1
EPIMED INTERNATIONAL, INC.
  SUBSTANTIALLY EQUIVALENT 1
HK SURGICAL
  SUBSTANTIALLY EQUIVALENT 1
JMT CO., LTD.
  SUBSTANTIALLY EQUIVALENT 1
TELEFLEX MEDICAL
  SUBSTANTIALLY EQUIVALENT 1

MDR Year MDR Reports MDR Events
2020 159 159
2021 146 152
2022 135 135
2023 79 79
2024 98 98
2025 124 124

Device Problems MDRs with this Device Problem Events in those MDRs
Break 185 188
Fluid/Blood Leak 66 66
Material Separation 64 64
Obstruction of Flow 56 56
Material Twisted/Bent 50 50
No Flow 41 41
Difficult to Advance 41 41
Failure to Advance 23 23
Physical Resistance/Sticking 21 21
Detachment of Device or Device Component 20 21
Adverse Event Without Identified Device or Use Problem 16 16
Material Fragmentation 16 18
Leak/Splash 14 14
Difficult to Remove 14 16
Material Split, Cut or Torn 12 12
Disconnection 11 11
Fracture 10 10
Unsealed Device Packaging 9 9
Material Integrity Problem 8 8
Stretched 8 8
Material Too Soft/Flexible 6 6
Complete Blockage 6 6
Burst Container or Vessel 5 5
Shipping Damage or Problem 5 5
Activation, Positioning or Separation Problem 4 4
Material Puncture/Hole 4 4
Defective Component 4 4
Defective Device 4 4
Premature Separation 3 3
Device Dislodged or Dislocated 3 3
Failure to Infuse 3 3
Material Rupture 3 3
Unraveled Material 3 3
Separation Problem 3 3
Device Damaged Prior to Use 3 3
Incomplete or Inadequate Connection 3 3
Dull, Blunt 2 2
Contamination 2 2
Unintended Movement 2 2
Gas/Air Leak 2 2
Entrapment of Device 2 2
Difficult to Flush 2 2
Flushing Problem 2 2
Device Markings/Labelling Problem 2 2
Material Deformation 2 2
Mechanical Problem 2 2
Crack 2 2
Device Contamination with Body Fluid 2 2
Component or Accessory Incompatibility 1 1
Pressure Problem 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 391 392
Foreign Body In Patient 110 112
No Consequences Or Impact To Patient 85 85
Insufficient Information 59 62
No Patient Involvement 28 28
Pain 21 21
Device Embedded In Tissue or Plaque 16 16
Needle Stick/Puncture 15 15
Unspecified Infection 6 6
No Information 6 6
Discomfort 6 6
No Known Impact Or Consequence To Patient 5 5
Headache 4 4
Inadequate Pain Relief 3 3
Bacterial Infection 3 3
Swelling/ Edema 3 3
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 2 2
Embolism/Embolus 2 2
Hematoma 2 2
Hemorrhage/Bleeding 2 2
Cerebrospinal Fluid Leakage 2 2
Spinal Column Injury 2 2
Paresthesia 2 2
Distress 1 1
Pulmonary Embolism 1 1
Low Oxygen Saturation 1 1
Eye Pain 1 1
Respiratory Insufficiency 1 1
Convulsion/Seizure 1 1
Perforation of Vessels 1 1
Unspecified Tissue Injury 1 1
Tachycardia 1 1
Abscess 1 1
Awareness during Anaesthesia 1 1
Dyspnea 1 1
Vomiting 1 1
Fever 1 1
Foreign Body Reaction 1 1
Cellulitis 1 1
Rupture 1 1
Purulent Discharge 1 1
Cramp(s) /Muscle Spasm(s) 1 1
Perforation 1 1
Muscle Weakness 1 1
Fungal Infection 1 1
Sepsis 1 1
No Code Available 1 1
Decreased Sensitivity 1 1
Hypersensitivity/Allergic reaction 1 1
Neuropathy 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Arrow International Inc II Jun-05-2020
2 Arrow International Inc II Feb-14-2020
3 Arrow International Inc II Jan-24-2020
4 Epimed International II Aug-18-2021
5 Epimed International, Inc. II Mar-18-2021
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