Health ProductsType I recall

QUETIAPINE XR : Affected lots may exceed the established acceptable intake limit for N-nitroso-desalkyl-quetiapine (NNAP)

· Published by Health Canada · Official notice

Details

Alert type: Health product recall
Category: Health products - Drugs
Product: QUETIAPINE XR
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
SIVEM PHARMACEUTICALS ULCQUETIAPINE XR/50MGDIN 02417359TabletQUETIAPINE (QUETIAPINE FUMARATE) 50 mgM2213000, M2213001, M2215146, M2214004
SIVEM PHARMACEUTICALS ULCQUETIAPINE XR/150MGDIN 02417367TabletQUETIAPINE (QUETIAPINE FUMARATE) 150 mgM2214685, M2214686, M2214687
SIVEM PHARMACEUTICALS ULCQUETIAPINE XR/200MGDIN 02417375TabletQUETIAPINE (QUETIAPINE FUMARATE) 200 mgM2214012, M2214013, M2214014
SIVEM PHARMACEUTICALS ULCQUETIAPINE XR/300MGDIN 02417383TabletQUETIAPINE (QUETIAPINE FUMARATE) 300 mgM2214016, M2214017, M2214018
SIVEM PHARMACEUTICALS ULCQUETIAPINE XR/400MGDIN 02417391TabletQUETIAPINE (QUETIAPINE FUMARATE) 400 mgM2214020

Issue

Affected lots may exceed the established acceptable intake limit for N-nitroso-desalkyl-quetiapine (NNAP).

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