• 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 ventilator, emergency, manual (resuscitator)
Regulation Description Manual emergency ventilator.
Product CodeBTM
Regulation Number 868.5915
Device Class 2


Premarket Reviews
ManufacturerDecision
ARCHEON
  SUBSTANTIALLY EQUIVALENT 1
COMPACT MEDICAL, INC.
  SUBSTANTIALLY EQUIVALENT 1
  1.  K243861  butterflyBVM
LAERDAL MEDICAL AS
  SUBSTANTIALLY EQUIVALENT 1
SAFE BVM CORPORATION
  SUBSTANTIALLY EQUIVALENT 1
XIAMEN COMPOWER MEDICAL TECH. CO., LTD.
  SUBSTANTIALLY EQUIVALENT 1

MDR Year MDR Reports MDR Events
2019 46 60
2020 26 26
2021 42 42
2022 35 35
2023 46 53
2024 33 33
2025 36 36

Device Problems MDRs with this Device Problem Events in those MDRs
Break 22 22
Inflation Problem 21 21
Defective Device 13 27
Defective Component 11 11
Deflation Problem 11 11
Gas/Air Leak 10 10
Detachment of Device or Device Component 10 10
Material Integrity Problem 10 10
Pressure Problem 9 9
Device Damaged Prior to Use 9 9
Component Missing 8 8
Connection Problem 7 7
Physical Resistance/Sticking 6 6
No Flow 6 6
Crack 6 27
Failure to Deliver 6 6
Incomplete or Inadequate Connection 5 5
Material Puncture/Hole 5 5
Failure to Seal 4 4
Material Split, Cut or Torn 4 4
Mechanical Problem 4 4
Infusion or Flow Problem 4 4
Material Deformation 4 4
Loose or Intermittent Connection 4 4
Difficult to Open or Close 4 4
Material Fragmentation 4 4
Unintended Deflation 4 4
Therapeutic or Diagnostic Output Failure 4 4
Obstruction of Flow 3 3
Use of Device Problem 3 3
Output Problem 3 3
Incomplete or Missing Packaging 3 3
Fluid/Blood Leak 3 3
Fitting Problem 3 3
Disconnection 3 3
Inadequacy of Device Shape and/or Size 2 2
Material Separation 2 2
Tear, Rip or Hole in Device Packaging 2 2
Device Handling Problem 2 2
Packaging Problem 2 2
Device Dislodged or Dislocated 2 2
Failure to Disconnect 2 2
No Device Output 2 2
Blocked Connection 2 2
Structural Problem 2 2
Material Twisted/Bent 2 2
Improper Flow or Infusion 2 2
Material Too Rigid or Stiff 2 2
Decrease in Pressure 1 1
Insufficient Flow or Under Infusion 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 77 80
No Known Impact Or Consequence To Patient 36 50
Insufficient Information 34 38
Low Oxygen Saturation 24 24
Cardiac Arrest 16 16
No Consequences Or Impact To Patient 15 15
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 14 14
No Patient Involvement 10 10
Hypoxia 5 5
Decreased Respiratory Rate 5 5
Death 4 4
Respiratory Insufficiency 4 4
Bradycardia 3 3
Unspecified Respiratory Problem 3 3
Loss of consciousness 3 3
Hypoventilation 2 2
No Code Available 2 2
Respiratory Arrest 2 2
Vomiting 2 2
Overinflation of Lung 2 2
Low Blood Pressure/ Hypotension 2 2
Respiratory Failure 2 2
Cerebral Edema 2 2
Pneumothorax 1 1
Failure of Implant 1 1
Respiratory Distress 1 1
No Information 1 1
Diminished Pulse Pressure 1 1
Anemia 1 1
Foreign Body In Patient 1 1
Dyspnea 1 1
Missing Value Reason 1 1
Asystole 1 1
Unspecified Tissue Injury 1 1
Endocarditis 1 1
Cardiovascular Insufficiency 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Ambu Inc. I Aug-13-2025
2 SunMed Holdings, LLC I May-30-2025
3 SunMed Holdings, LLC II Nov-21-2023
4 Vyaire Medical I Feb-25-2024
-
-