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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device blood establishment computer software and accessories
Regulation Description Blood establishment computer software and accessories.
Product CodeMMH
Regulation Number 864.9165
Device Class 2


Premarket Reviews
ManufacturerDecision
BLOOD BANK COMPUTER SYSTEMS, INC.
  SUBSTANTIALLY EQUIVALENT 2
CARTER BLOODCARE
  SUBSTANTIALLY EQUIVALENT 2
CSL PLASMA
  SUBSTANTIALLY EQUIVALENT 1
DATA INNOVATIONS LLC
  SUBSTANTIALLY EQUIVALENT 1
DEPARTMENT OF VETERANS AFFAIRS
  SUBSTANTIALLY EQUIVALENT 1
EPIC
  SUBSTANTIALLY EQUIVALENT 2
EPIC SYSTEMS CORPORATION
  SUBSTANTIALLY EQUIVALENT 2
GRIFOLS DIAGNOSTIC SOLUTIONS INC.
  SUBSTANTIALLY EQUIVALENT 1
HAEMONETICS CORP.
  SUBSTANTIALLY EQUIVALENT 5
HAEMONETICS CORPORATION
  SUBSTANTIALLY EQUIVALENT 5
HEALTHCARE-ID, INC.
  SUBSTANTIALLY EQUIVALENT 3
IMMUCOR, INC.
  SUBSTANTIALLY EQUIVALENT 1
MEDICAL INFORMATION TECHNOLOGY, INC.
  SUBSTANTIALLY EQUIVALENT 1
MEDIWARE INFORMATION SYSTEMS, INC.
  SUBSTANTIALLY EQUIVALENT 2
STRATEC BIOMEDICAL UK LIMITED
  SUBSTANTIALLY EQUIVALENT 1
SUNQUEST INFORMATION SYSTEMS, INC.
  SUBSTANTIALLY EQUIVALENT 2

MDR Year MDR Reports MDR Events
2015 3 3
2016 9 9
2017 8 8
2018 12 12
2019 10 10
2020 1 1

Device Problems MDRs with this Device Problem Events in those MDRs
Computer Software Problem 8 8
Patient Data Problem 5 5
Nonstandard Device 4 4
Application Program Problem 4 4
Improper or Incorrect Procedure or Method 4 4
Use of Device Problem 3 3
Programming Issue 3 3
Insufficient Information 2 2
Incorrect Software Programming Calculations 2 2
Device Operates Differently Than Expected 2 2
Data Problem 2 2
Failure to Convert to Back-Up 1 1
Loss of Data 1 1
Device Markings/Labelling Problem 1 1
Adverse Event Without Identified Device or Use Problem 1 1
Application Program Problem: Dose Calculation Error 1 1
Device Difficult to Program or Calibrate 1 1
Failure to Transmit Record 1 1
Device Operational Issue 1 1
Output Problem 1 1
Problem with Software Installation 1 1
Smoking 1 1
Communication or Transmission Problem 1 1
Incorrect Or Inadequate Test Results 1 1
Sparking 1 1
Application Network Problem 1 1
No Device Output 1 1
Use of Incorrect Control Settings 1 1
False Positive Result 1 1
Appropriate Term/Code Not Available 1 1
Protective Measures Problem 1 1
Device Component Or Accessory 1 1
Application Program Problem: Medication Error 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Known Impact Or Consequence To Patient 19 19
Death 5 5
No Patient Involvement 4 4
No Consequences Or Impact To Patient 4 4
No Information 3 3
Overdose 3 3
No Code Available 2 2
Not Applicable 1 1
Tachycardia 1 1
Blurred Vision 1 1
Dizziness 1 1
Toxicity 1 1
Loss of consciousness 1 1
Sweating 1 1
Palpitations 1 1
Fatigue 1 1
Swelling 1 1
Therapeutic Effects, Unexpected 1 1

Recalls
Manufacturer Recall Class Date Posted
1 ConvaTec, Inc II May-16-2018
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