Lifeworks Technology Massage Guns Recalled as Unauthorised Device
Summary
Health Canada has recalled Lifeworks Technology Vibra-Heal and Restore Massage Guns because they were distributed without a valid medical device licence. Sales have ceased, and the company plans to apply for the necessary licence.
What changed
Health Canada has issued a Type II recall for Lifeworks Technology Vibra-Heal and Restore Massage Guns. The devices were distributed in Canada without a valid Class II Medical Device Licence, violating the Medical Devices Regulations. While no safety defect has been identified, sales of the affected products have been halted, and the manufacturer intends to pursue the required licensing.
Companies involved in the distribution or sale of these massage guns should cease all sales immediately and contact the manufacturer for further information. While no specific compliance deadline is mentioned, the immediate cessation of sales and the planned licence application indicate a need for prompt action to rectify the regulatory non-compliance. Failure to comply with medical device regulations can lead to further enforcement actions.
What to do next
- Cease all sales of Lifeworks Technology Vibra-Heal and Restore Massage Guns.
- Contact Lifeworks Technology Group, LLC for further information regarding the recall and licensing process.
Source document (simplified)
Health product recall
Lifeworks Technology Vibra-Heal and Restore Massage Guns
Brand(s)
Lifeworks Technology Group, LLC
Last updated
2026-03-05
Summary
Product Lifeworks Technology Vibra-Heal and Restore Massage Guns Issue Medical devices - Unauthorised device What to do Contact the manufacturer if you require additional information.
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
| --- | --- | --- |
| Vibra-Heal Deep Tissue Massage Gun | All lots. | 4RBRR0261B0G7 |
| Restore Deep Tissue Travel Massage Gun | All lots. | 4RBRR0292B0G7 |
Issue
The device was distributed in Canada without a valid class II Medical Device Licence under the Medical Devices Regulations. No safety defect has been identified. Sales ceased and a licence application is planned.
Additional information
Details
Original published date:
2026-03-05
Alert / recall type Health product recall Category Health products - Medical devices - Physical medicine Companies Lifeworks Technology Group, LLC
530 Seventh Avenue, Floor 21, New York, New York, United States, 10018
Published by Health Canada Audience General public Recall class Type II Recall date
2026-02-11
Identification number RA-81698
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