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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
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
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