Recall Monitor
Health ProductsType I recall

PRO-FLUOXETINE: Affected lots exceed the interim acceptable limit for N-nitroso-fluoxetine.

· Published by Health Canada · Official notice

Details

Alert type: Health product recall
Category: Health products - Drugs
Product: PRO-FLUOXETINE
Issue: Health products - Product quality
What to do: Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health concerns.
Distribution: National
Audience: General public, Healthcare, Industry
Recall class: Type I
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Products

BrandProduct NameMarket AuthorizationDosage FormStrengthLot numbers
Pro Doc LimitéePRO-FLUOXETINE 10mgDIN 02314991CapsulesFLUOXETINE (FLUOXETINE HYDROCHLORIDE) 10mg648684, 648064, 646136, 645497, 644908, 643212 & 641894
Pro Doc LimitéePRO-FLUOXETINE 20mgDIN 02315009CapsulesFLUOXETINE (FLUOXETINE HYDROCHLORIDE) 20mg642181

Issue

The affected lots exceed the interim acceptable intake limit for N-nitroso-fluoxetine.

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