Recall Monitor
Health ProductsType I recall

PRO-Fluoxetine 10 mg capsule; may exceed the interim acceptable intake limit for N-nitroso-fluoxetine

· Published by Health Canada · Official notice

Details

Alert type: Health product recall
Category: Health products - Drugs
Product: PRO-Fluoxetine 10 mg capsule
Issue: Health products - Product quality
What to do: Consult your health care professional if you have any health concerns.
Audience: General public, Healthcare, Industry
Recall class: Type I
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Products

BrandProduct NameMarket AuthorizationDosage FormStrengthLot number
Pro Doc LimitéePRO-Fluoxetine 10 mg capsuleDIN 02314991CapsuleFluoxetine hydrochloride 10 mg651194, 656543, 658509, 659876

Issue

Affected lots may exceed the interim acceptable intake limit for N-nitroso-fluoxetine.

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