Sani-Derm: may contain DA-21 Ethanol
Last updated
Summary
Product
Sani-Derm
Issue
Health products - Product safety
What to do
See instructions below.
Affected products
| Brand | Product Name | Market Authorization | Dosage Form | Strength | Lot |
|---|---|---|---|---|---|
| Sani-Derm | Sani-Derm | No Market Authorization | Gel | Sani-Derm 62% w/w (70% v/v) Ethyl alcohol (Ethanol) | 02825, 03425, 03725, 05925, 06225, 06425, 06925, 07125, 07325, 07825, 07925, 08025, 08325, 08425, 08525, 08625, 08825, 09025, 09125, 09525, 09825, 09925, 10525, 10625 |
Issue
| The affected lots could contain type DA-21 ethanol. |
What you should do
- Verify if your product is affected.
- Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health concerns.
- Contact the recalling firm if you have any questions about the recall.
- Report any health product related side effects to Health Canada.
- Report any other health product safety complaints to Health Canada.
Additional information
Previous recalls or alerts
Background
Depth of recall: Retailers
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Natural health products
Companies
|
Laboratoires Choisy (Kersia Group). 390, Boul. Saint-Laurent Est, C.P 6 Louiseville, Quebec, J5V 2L7 |
Published by
Health Canada
Audience
General public
Health professionals
Hospitals
Recall class
Type II
Identification number
RA-63725
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