Two Lots Of Mar-amlodipine 5 Mg Tablets Recalled As Some Bottles May Contain The Wrong Drug
Two batches of MAR-Amlodipine 5 mg tablets are being recalled in Canada because some bottles may contain the wrong medication instead of amlodipine. The affected product is identified by DIN 02371715 and was distributed across Canada. Consumers who have this medication should check if their bottle is from one of the recalled lots.
- Product
- MAR-Amlodipine 5 mg, DIN 02371715
- Reason
- Product safety concern
- Category
- consumer product recall
- Country
- Canada
- Agency
- HC-PRODUCTS
- Recall date
- 2026-02-07
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-PRODUCTS
Recall details on Nibble Recalls: https://trynibble.app/recalls/822bb0e5-0c41-400d-959b-d4da01f16bbb