Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Medicine |
| Medsafe Reference: | 22352 |
| Brand Name: | Leustatin |
| Dose Form/Strength: | Solution for infusion 1 mg/mL |
| Affected: | LOT: HBZS702 |
| Recalling Organisation: | Janssen-Cilag (New Zealand) Ltd 507 Mt Wellington Highway AUCKLAND 1060 |
| Contact Information: | 0800 800 806 |
| Manufacturer: | GlaxoSmithKline Manufacturing SpA |
| Issue: | Janssen-Cilag New Zealand Limited is conducting a recall of one lot of Leustatin Injection due to a manufacturing deviation that can lead to a lower assay value for a small number of vials of this batch. |
| Recall action type: | Recall |
| Recall action: | Recall |
| Level of recall: | Wholesale |
| Date Commenced: | 14/12/2017 |
