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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Product CodeILQ
Regulation Number 890.3710
Device Class 2

MDR Year MDR Reports MDR Events
2019 2 2
2020 2 2
2021 5 5
2022 27 27
2023 74 74
2024 19 19

Device Problems MDRs with this Device Problem Events in those MDRs
Device Alarm System 89 89
No Audible Alarm 13 13
Defective Alarm 5 5
Use of Device Problem 3 3
Defective Device 2 2
Application Program Problem 2 2
Temperature Problem 2 2
Wireless Communication Problem 2 2
Activation Problem 2 2
Communication or Transmission Problem 2 2
Activation, Positioning or Separation Problem 1 1
Human-Device Interface Problem 1 1
Inadequate User Interface 1 1
Lack of Maintenance Documentation or Guidelines 1 1
Adverse Event Without Identified Device or Use Problem 1 1
Output Problem 1 1
Protective Measures Problem 1 1
Delayed Alarm 1 1
False Alarm 1 1
Alarm Not Visible 1 1
Break 1 1
Overheating of Device 1 1
Device Difficult to Program or Calibrate 1 1
Product Quality Problem 1 1
Misassembled During Installation 1 1
Unexpected Shutdown 1 1
Therapeutic or Diagnostic Output Failure 1 1
Application Program Version or Upgrade Problem 1 1
Defective Component 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 111 111
Insufficient Information 6 6
Fall 4 4
No Known Impact Or Consequence To Patient 3 3
Laceration(s) 1 1
Superficial (First Degree) Burn 1 1
Abrasion 1 1
Cardiac Arrest 1 1
Death 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Baxter Healthcare Corporation II Jun-30-2022
2 Baxter Healthcare Corporation II May-13-2022
3 Forbes Rehab Services Inc II Dec-28-2021
4 Hill-Rom Inc. II Dec-20-2021
5 Medminder Systems, Inc. II Jun-09-2022
6 Tobii Dynavox Llc II Apr-18-2023
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