Sani-Derm: may contain DA-2I Ethanol

Last updated

2021-12-22

View history

Summary

Product

Sani-Derm

Issue

Health products - Product safety

What to do

See instructions below.

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)	0282510, 0342505, 0372502, 0592507, 0592514, 0622501, 0622502, 0642509, 0692510, 0712501, 0712504, 0712505, 0712507, 0732505, 0732506, 0782511, 0782512, 0782518, 0792514, 0792517, 0792519, 0802504, 0802505, 0802508, 0802510, 0832508, 0842509, 0852502, 0852509, 0852510, 0852514, 0852517, 0862502, 0862506, 0882501, 0902511, 0902512, 0912501, 0912502, 0912503, 0952501, 0952502, 0982507, 0992504, 0992507, 0992508, 0992509, 1052515, 1062502, 1062504, 1062505, 1062508, 1082507, 1112516

The affected lots could contain type DA-2I ethanol.

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.

Previous recalls or alerts

Background

Depth of recall: Retailers

Details

Original published date: 2021-12-15

Alert / recall type

Health product recall

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