Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Medicine |
| Medsafe Reference: | 22754 |
| Brand Name: | Reminyl Prolonged Release Capsules |
| Dose Form/Strength: | Modified release capsule 8 mg |
| Affected: | HALDE00, HALDE01, HALDE02 and HALDE03 |
| Recalling Organisation: | Janssen-Cilag (New Zealand) Ltd 507 Mt Wellington Highway AUCKLAND 1060 |
| Contact Information: | 0800 800 806 |
| Manufacturer: | Janssen-Cilag SpA |
| Issue: | An Out of Specification result for assay of Galantamine Hydrobromide was obtained during long-term stability monitoring. |
| Recall action type: | Recall |
| Recall action: | Recall |
| Level of recall: | Wholesale |
| Date Commenced: | 27/4/2018 |
