Recall Monitor
Health ProductsType I recall

PMS-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: PMS-FLUOXETINE 10mg
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
PharmasciencePMS-FLUOXETINE 10mgDIN 02177579CapsulesFLUOXETINE (FLUOXETINE HYDROCHLORIDE) 10mg644913, 643517, 648104, 646137, 653478, 648683, 648063, 648065, 647542, 641417, 641895, 646134, 644911, 643518, 643213, 645409, 642179, 644912, 642513, 655449, 649562, 648682, 651196, 653477, 648067, 647317, 645496, 646133, 645498, 646135 & 648066
PharmasciencePMS-FLUOXETINE 20mgDIN 02177587CapsulesFLUOXETINE (FLUOXETINE HYDROCHLORIDE) 20mg644549, 645412, 642182 & 641413

Issue

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

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