Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Medicine |
| Medsafe Reference: | 20958 |
| Brand Name: | Mirena |
| Dose Form/Strength: | Intrauterine contraceptive device 52 mg (releases 20µg/24h) |
| Affected: | TU01BT0 |
| Recalling Organisation: | Bayer New Zealand Limited Consumer Health B:Hive Building 74 Tahoroto Rahoto, Takapuna Auckland 0622 |
| Contact Information: | 0800 804 545 |
| Manufacturer: | Bayer Oy |
| Issue: | Potential for inversely mounted insertion tubes on some units. |
| Recall action type: | Recall |
| Recall action: | Recall |
| Level of recall: | Healthcare Professional |
| Date Commenced: | 13/1/2017 |
