• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

New Search show TPLC since Back to Search Results
Device restraint, protective
Regulation Description Protective restraint.
Product CodeFMQ
Regulation Number 880.6760
Device Class 1

MDR Year MDR Reports MDR Events
2021 33 33
2022 54 54
2023 47 47
2024 58 58
2025 15 15
2026 6 6

Device Problems MDRs with this Device Problem Events in those MDRs
Break 61 61
Device Slipped 37 37
Material Split, Cut or Torn 11 11
Mechanical Problem 11 11
Insufficient Information 9 9
Adverse Event Without Identified Device or Use Problem 8 8
Patient Device Interaction Problem 7 7
Material Frayed 5 5
Defective Component 5 5
Use of Device Problem 5 5
Labelling, Instructions for Use or Training Problem 5 5
Material Disintegration 4 4
Defective Device 4 4
Positioning Problem 4 4
Product Quality Problem 4 4
Human-Device Interface Problem 4 4
Difficult to Open or Close 4 4
Activation, Positioning or Separation Problem 3 3
Material Integrity Problem 3 3
Fail-Safe Problem 3 3
Device Handling Problem 3 3
Connection Problem 3 3
Material Puncture/Hole 2 2
Difficult or Delayed Separation 2 2
Appropriate Term/Code Not Available 2 2
Disconnection 1 1
Off-Label Use 1 1
Crack 1 1
Unintended Movement 1 1
Therapeutic or Diagnostic Output Failure 1 1
Inadequate Instructions for Healthcare Professional 1 1
Material Separation 1 1
Inadequacy of Device Shape and/or Size 1 1
Detachment of Device or Device Component 1 1
Device Dislodged or Dislocated 1 1
Protective Measures Problem 1 1
Material Too Soft/Flexible 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 152 152
Insufficient Information 22 22
Irritability 6 6
Unspecified Mental, Emotional or Behavioural Problem 5 5
Unintended Extubation 5 5
Loss of consciousness 2 2
Choking 2 2
Emotional Changes 2 2
No Consequences Or Impact To Patient 2 2
Bone Fracture(s) 2 2
Head Injury 1 1
Laceration(s) 1 1
Damage to Ligament(s) 1 1
Pain 1 1
Paresis 1 1
Concussion 1 1
Abrasion 1 1
Airway Obstruction 1 1
Aspiration/Inhalation 1 1
Cardiac Arrest 1 1
Death 1 1
Anxiety 1 1
Ventilator Dependent 1 1
Extubate 1 1
Numbness 1 1
Fall 1 1
Needle Stick/Puncture 1 1
Low Oxygen Saturation 1 1
Confusion/ Disorientation 1 1
Foreign Body In Patient 1 1
Unspecified Tissue Injury 1 1
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 1 1

Recalls
Manufacturer Recall Class Date Posted
1 DeRoyal Industries Inc II Aug-22-2022
2 Queen Comfort Products lLC II Nov-01-2021
-
-