Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Medicine |
| Medsafe Reference: | 26042 |
| Brand Name: | Duavive |
| Dose Form/Strength: | Modified release tablet 0.45mg/20mg |
| Affected: | DG3961, AW3843, W46903, X89874 |
| Recalling Organisation: | Pfizer New Zealand Limited C/-ICON Clinical Research New Zealand Ltd Plaza Level, c/-Regus 41 Shortland Street AUCKLAND 1010 |
| Contact Information: | 0800 734 076 |
| Manufacturer: | Pfizer Ireland Pharmaceuticals Unlimited Company |
| Issue: | Pfizer is recalling batches of Duavive tablets to wholesale level due to an out of specification result for the finished product. The out of specification may result in a low dissolution time for bazedoxifene. |
| Recall action type: | Recall |
| Recall action: | Recall |
| Level of recall: | Wholesale |
| Date Commenced: | 25/5/2020 |
