Sandoz-Valsartan Product Recall (2021-05-27)
· Published by Health Canada · Official notice
Alert type: Drug Recall
Category: Drugs
Issue: Product Safety
Audience: General Public, Healthcare Professionals, Hospitals
Department: Health Canada
Hazard classification: Type I
Sandoz Valsartan 80mg Tablet
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| Lot or serial number | Companies | Brand name | DIN, NPN, DIN-HIM | Dosage form | Strength |
|---|
| KT9598 | - Recalling Firm
- Sandoz Canada Inc
- 110 de Lauzon
- Boucherville
- J4B 1E6
- Quebec
- CANADA
- Marketing Authorization Holder
- Sandoz Canada Inc
- 110 de Lauzon
- Boucherville
- J4B 1E6
- Quebec
- CANADA
| B. Sandoz Valsartan 160mg Tablet | DIN 02356767 | Tablet | Valsartan 160mg |
| KT8923, KV6185 | - Recalling Firm
- Sandoz Canada Inc
- 110 de Lauzon
- Boucherville
- J4B 1E6
- Quebec
- CANADA
- Marketing Authorization Holder
- Sandoz Canada Inc
- 110 de Lauzon
- Boucherville
- J4B 1E6
- Quebec
- CANADA
| C. Sandoz Valsartan 320mg Tablet | DIN 02356775 | Tablet | Valsartan 320mg |
| KT7180, KT9515 | - Recalling Firm
- Sandoz Canada Inc
- 110 de Lauzon
- Boucherville
- J4B 1E6
- Quebec
- CANADA
- Marketing Authorization Holder
- Sandoz Canada Inc
- 110 de Lauzon
- Boucherville
- J4B 1E6
- Quebec
- CANADA
| A. Sandoz Valsartan 80mg Tablet | DIN 02356759 | Tablet | Valsartan 80mg |
-
Sandoz Valsartan 80mg Tablet
-
Sandoz Valsartan 160mg Tablet
-
Sandoz Valsartan 320mg Tablet
Presence of impurity 5-(4-(azidomethyl)-[1,1-biphenyl]-2-yl)-1H-tetrazole above the acceptable concentration limit in affected lots.