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Device
ventilator, emergency, manual (resuscitator)
Regulation Description
Manual emergency ventilator.
Product Code
BTM
Regulation Number
868.5915
Device Class
2
Premarket Reviews
Manufacturer
Decision
ARCHEON
SUBSTANTIALLY EQUIVALENT
1
1. K221841
EOlife®
COMPACT MEDICAL, INC.
SUBSTANTIALLY EQUIVALENT
1
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
2020
26
26
2021
42
42
2022
35
35
2023
46
53
2024
33
33
2025
36
36
2026
17
17
Device Problems
MDRs with this Device Problem
Events in those MDRs
Break
21
21
Inflation Problem
15
15
Gas/Air Leak
15
15
Material Integrity Problem
12
12
Defective Device
10
10
Deflation Problem
10
10
Pressure Problem
8
8
Detachment of Device or Device Component
7
7
Failure to Deliver
6
6
Physical Resistance/Sticking
6
6
Crack
6
13
Material Fragmentation
6
6
Incomplete or Inadequate Connection
5
5
No Flow
5
5
Defective Component
5
5
Component Missing
5
5
Difficult to Open or Close
4
4
Infusion or Flow Problem
4
4
Therapeutic or Diagnostic Output Failure
4
4
Material Split, Cut or Torn
4
4
Unintended Deflation
4
4
Failure to Seal
4
4
Material Puncture/Hole
4
4
Disconnection
4
4
Fluid/Blood Leak
3
3
Mechanical Problem
3
3
Use of Device Problem
3
3
Loose or Intermittent Connection
3
3
Material Deformation
3
3
Output Problem
3
3
Obstruction of Flow
3
3
Structural Problem
2
2
Blocked Connection
2
2
Connection Problem
2
2
Incomplete or Missing Packaging
2
2
Tear, Rip or Hole in Device Packaging
2
2
Improper Flow or Infusion
2
2
Device Dislodged or Dislocated
2
2
Packaging Problem
2
2
Material Twisted/Bent
2
2
Insufficient Information
2
2
Device Handling Problem
2
2
No Device Output
2
2
Decrease in Pressure
2
2
Material Too Rigid or Stiff
2
2
Material Separation
2
2
Inadequacy of Device Shape and/or Size
2
2
Fitting Problem
2
2
Leak/Splash
2
2
Misassembled
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Clinical Signs, Symptoms or Conditions
86
89
Insufficient Information
35
39
Low Oxygen Saturation
25
25
Cardiac Arrest
17
17
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available
16
16
No Known Impact Or Consequence To Patient
12
12
No Consequences Or Impact To Patient
9
9
Hypoxia
6
6
Respiratory Insufficiency
5
5
Decreased Respiratory Rate
5
5
Hypoventilation
3
3
Bradycardia
3
3
Unspecified Respiratory Problem
3
3
Loss of consciousness
3
3
Respiratory Failure
3
3
Respiratory Arrest
2
2
Vomiting
2
2
Overinflation of Lung
2
2
Low Blood Pressure/ Hypotension
2
2
Cerebral Edema
2
2
Death
1
1
Pneumothorax
1
1
Failure of Implant
1
1
No Code Available
1
1
No Information
1
1
Diminished Pulse Pressure
1
1
Anemia
1
1
Foreign Body In Patient
1
1
Dyspnea
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
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