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TPLC
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Device
catheter, conduction, anesthetic
Regulation Description
Anesthesia conduction catheter.
Product Code
BSO
Regulation Number
868.5120
Device Class
2
Premarket Reviews
Manufacturer
Decision
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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