Official recall record
MediHoney® Leptospermum Honey Tube
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-10-23
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
There are potential for pinholes in the applicator pouch film which creates a sterility concern. Manufacturer reported that there have been 4 complaints reported worldwide with the potential to be related to this sterility concern as of 08/05/2024, none of which alleged serious injury or deaths. Additionally, these products were found to be unlicensed for sale in Canada and were distributed without a license. Recall start date: September 16, 2024
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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