Public recall detail

Unlicensed soft-shelled hyperbaric chambers may pose serious health risks

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Recall Safety notice
Quick summary

Quick summary: Unlicensed soft-shelled hyperbaric chambers may pose serious health risks .

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Unlicensed soft-shelled hyperbaric chambers may pose serious health risks .

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

Brand
ProductUnlicensed soft-shelled hyperbaric chambers
IssueHealth products - Unauthorized product
IdentificationRA-61813

Affected products

ProductUnlicensed soft-shelled hyperbaric chambers
DescriptionIn early 2020, Health Canada seized six unlicensed soft-shelled hyperbaric chamber units from distributors in the Province of Quebec. The models are:Yada Vertical Soft Shell Hyperbaric Chamber and Yada Horizontal Soft Shell Hyperbaric Chamber, manufactured by YadaVitaeris 320 Horizontal Soft Shell Hyperbaric Chamber, manufactured by Oxyhealth LLC.Oxynova Serie 9 Horizontal Soft Shell Hyperbaric Chamber, manufactured by OxynovaIn September 2020, the Department seized three more unlicensed soft-shelled hyperbaric chamber units from a distributor in Alberta. The models are:Oxynova serie 7 Soft Shell Hyperbaric Chamber, manufactured by OxynovaOxynova serie 8 Soft Shell Hyperbaric Chamber, manufactured by OxynovaOxynova serie 9 Soft Shell Hyperbaric Chamber, manufactured by Oxynova

Issue

Health Canada is advising Canadians that soft-shelled hyperbaric chambers that are promoted online or offered as a service to consumers to treat a variety of medical conditions including autism, cerebral palsy and migraines are unlicensed medical devices and may pose serious health risks.Soft-shelled hyperbaric chambers may expose patients, or those in close proximity, to serious injury, including death. Risks include fire, spreading transmissible diseases through cross-contamination between users, damage to the ears, eyes, sinuses, lungs and teeth, and changes to blood sugar levels. The risk of fire is significantly increased when the device is used in combination with an oxygen concentration device.Since first warning Canadians about the risks of using unlicensed soft-shelled hyperbaric chambers in October 2019, the Department has continued to take action to remove these products from the market and to respond to complaints.Health Canada will continue to take action with companies (importers, distributors and manufacturers) selling unlicensed soft-shelled hyperbaric chambers. Health Canada is also working with the Canada Border Services Agency to help prevent further illegal importation of unlicensed soft-shelled hyperbaric chambers.It is illegal to advertise for sale, import for sale, or sell medical devices in Canada without appropriate licensing, under the Medical Devices Regulations.While Health Canada has not licensed any soft-shelled hyperbaric chambers, oxygen therapy using hard-shelled hyperbaric chambers is a well-established medical treatment where patients are placed in an oxygen-rich and pressurized environment. Health Canada has licensed four hard-shelled hyperbaric chamber manufacturers in Canada.To learn more about hard-shelled hyperbaric chambers, visit Health Canada's Hyperbaric Oxygen Therapy webpage.

What you should do

  • Do not purchase soft-shelled hyperbaric chambers online or obtain treatment from third parties using these products.
  • Consult your healthcare practitioner if you use or have used a soft-shelled hyperbaric chamber and you have concerns about your health.
  • Check whether medical devices have been licensed for sale by searching Health Canada's Medical Devices Active Licence Listing.
  • Report complaints involving medical devices, including the sale of unlicensed devices, to Health Canada.
  • Stay connected with Health Canada and receive the latest advisories and product recalls.
Additional official information
AudienceGeneral public
CategoryHealth products - Medical devices
CompaniesPublished by Health Canada
Published byHealth Canada
Alert / recall typePublic advisory
Identification numberRA-61813
Background{}
CompaniesPublished by Health Canada
AudiencesGeneral public
Source updated2020-11-06

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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