The FDA doesn’t want people to buy and use anti-choking devices. They recommend using established choking rescue protocols instead.
The safety and effectiveness of over-the-counter choking devices have not been established. This device has not been approved or cleared by the FDA.
The FDA is concerned that using an anti-choking device for the first time could lead to choking for longer because it takes time to remove the device from the package, assemble it, and follow the instructions.
The FDA stated that the following issues have been reported with anti-choking devices:
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This device did not prevent suffocation due to lack of suction.
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Bruises appear on the face, lips, and around the mouth.
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A scratch on the back of my throat.
It is recommended that you follow asphyxiation rescue protocols approved by the American Red Cross and American Heart Association before considering using anything else. The Red Cross and AHA protocols have a high success rate and can be completed quickly.
What to do if someone is choking?
The FDA recommends following choking rescue procedures approved by the American Red Cross and American Heart Association.
Choking rescue protocols should only be used if the airway is completely obstructed or if you are unable to cough. That’s because a blow from the back can turn a partial airway obstruction that would normally resolve itself into a complete airway obstruction.
Use an anti-choking device only if approved protocols have been unsuccessful.
What does the FDA do?
FDA works with anti-asphyxiant manufacturers to ensure that their products comply with FDA medical device requirements.
How to report a problem with an anti-choking device
If you experience a problem while using an anti-choking device, you are asked to report it through: MedWatch Voluntary Report Form.
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