Vita Health Products Inc Ranitidine Product Recall (2019-10-24)Health ProductsOct 24th, 2019 @ 12:00 AM
Basic Details
Issue: Product Safety
Category: Drugs
Audience: General Public, Healthcare Professionals, Hospitals
Department: Health Canada
Hazard classification: Type I
Alert type: Drug Recall
Products
| Lot or serial number | Brand name | Companies | DIN, NPN, DIN-HIM | Dosage form | Strength |
|---|---|---|---|---|---|
| All lots | B. Maximum Strength Acid Reducer 150mg (Equate , iPharma, Western Family) |
| DIN 02298902 | Tablet | Ranitidine hydrochloride 150 mg |
| All lots | A. Acid Reducer 75mg (Equate, Stanley, Western Family, iPharma) |
| DIN 02298740 | Tablet | Ranitidine hydrochloride 75mg |
Introduction
A. Acid Reducer 75mg (Equate, Stanley, Western Family, iPharma)
B. Maximum Strength Acid Reducer 150mg (Equate , iPharma, Western Family)
Reason
Affected lots may be manufactured with an API containing an impurity, N-nitrosodimethylamine (NDMA)
Depth of distribution
Retailers
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