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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device apparatus, autotransfusion
Regulation Description Autotransfusion apparatus.
Product CodeCAC
Regulation Number 868.5830
Device Class 2


Premarket Reviews
ManufacturerDecision
ATRIUM MEDICAL CORPORATION
  SUBSTANTIALLY EQUIVALENT 1
FRESENIUS KABI AG
  SUBSTANTIALLY EQUIVALENT 1
HAEMONETICS CORPORATION
  SUBSTANTIALLY EQUIVALENT 1
  1.  K221722  Haemonetics Cell Saver Elite/Elite+ Autotransfusio ...
INARI MEDICAL
  SUBSTANTIALLY EQUIVALENT 1
INARI MEDICAL, INC.
  SUBSTANTIALLY EQUIVALENT 2
INQUIS MEDICAL
  SUBSTANTIALLY EQUIVALENT 1
SISU GLOBAL HEALTH
  SUBSTANTIALLY EQUIVALENT 1
SORIN GROUP ITALIA S.R.L.
  SUBSTANTIALLY EQUIVALENT 2

MDR Year MDR Reports MDR Events
2021 73 73
2022 65 69
2023 39 39
2024 129 137
2025 128 128
2026 67 67

Device Problems MDRs with this Device Problem Events in those MDRs
Fluid/Blood Leak 190 190
Mechanical Problem 85 85
Material Deformation 43 43
Crack 39 39
Optical Problem 35 35
Material Integrity Problem 31 31
Obstruction of Flow 27 27
Noise, Audible 23 23
Device Alarm System 23 23
Electrical /Electronic Property Problem 21 21
Device Misassembled During Manufacturing /Shipping 15 15
Nonstandard Device 15 15
Material Puncture/Hole 13 13
Insufficient Device Problem Information 12 12
Air/Gas in Device 11 11
Adverse Event Without Identified Device or Use Problem 9 9
Delivered as Unsterile Product 8 8
Break 7 7
No Apparent Adverse Event 5 6
Material Separation 4 4
Smoking 4 4
Use of Device Problem 3 3
Detachment of Device or Device Component 3 11
Appropriate Device Problem Term/Code Not Available 3 3
Contamination 2 2
Material Twisted/Bent 2 2
Leak/Splash 2 2
Connection Problem 2 2
Fracture 2 2
Suction Problem 2 2
Disconnection 2 2
Infusion or Flow Problem 2 2
Burst Container or Vessel 2 2
Application Program Freezes or Fails to Launch 1 1
Temperature Problem 1 1
Gas/Air Leak 1 1
Incorrect Measurement 1 1
Off-Label Use 1 1
Overheating of Device 1 1
Sharp Edges 1 1
Free or Unrestricted Flow 1 1
Power Problem 1 1
Increase in Suction 1 1
Blocked Connection 1 1
Chemical Problem 1 1
Unclear Information 1 1
Misassembled During Installation 1 1
Unsealed Device Packaging 1 1
Decrease in Suction 1 1
Manufacturing, Packaging or Shipping Problem 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 361 372
Hemorrhage/Blood Loss/Bleeding 146 146
Insufficient Information 16 18
Unspecified Blood or Lymphatic problem 12 12
Hypovolemia 5 5
Hemolysis 5 5
Perforation of Vessels 3 3
Low Cardiac Output 3 3
Low Blood Pressure/ Hypotension 3 3
Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available 3 3
Unspecified Tissue Injury 2 2
Pneumothorax 2 2
Thrombosis/Thrombus 2 2
Renal Failure 2 2
Bradycardia 2 2
Cognitive Changes 1 1
Ruptured Aneurysm 1 1
No Information 1 1
Pulmonary Embolism 1 1
Blister 1 1
Anemia 1 1
Low Oxygen Saturation 1 1
Inflammation 1 1
Aspiration Pneumonitis 1 1
Post Operative Wound Infection 1 1
Local Reaction 1 1
No Consequences Or Impact To Patient 1 1
Cardiac Arrest 1 1
Myocardial Contusion 1 1
Dyspnea 1 1
Cough 1 1
Unspecified Heart Problem 1 1
Kidney injury 1 1
Skin Tears 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Atrium Medical Corporation II Dec-28-2023
2 Atrium Medical Corporation II Dec-02-2023
3 Atrium Medical Corporation II Nov-16-2023
4 Maquet Cardiovascular, LLC I Jan-12-2024
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