Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Medicine |
| Medsafe Reference: | 36579 |
| Brand Name: | Arixtra (Onelink) |
| Dose Form/Strength: | Solution for injection 7.5 mg/0.6mL |
| Affected: | |
| Recalling Organisation: | Onelink 56 Carrington Road Pt Chevalier AUCKLAND |
| Contact Information: | (09) 815 2686 |
| Manufacturer: | |
| Issue: | Viatris(MAH) has received reports of brown discolouration and blockage in the needle of pre-filled syringes of Arixtra. This quality defect is related to oxidation of the syringe needle. |
| Recall action type: | Communication to healthcare professionals |
| Recall action: | Product alert |
| Level of recall: | Healthcare Professional |
| Date Commenced: | 18/3/2026 |
