Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Medicine |
| Medsafe Reference: | 26182 |
| Brand Name: | Herceptin |
| Dose Form/Strength: | Powder for infusion concentrate 440 mg |
| Affected: | |
| Recalling Organisation: | Roche Products (NZ) Ltd 98 Carlton Gore Road Newmarket Auckland 1023 |
| Contact Information: | |
| Manufacturer: | Genentech, Inc. |
| Issue: | Roche Products (New Zealand) Ltd is conducting an urgent hospital level recall of one batch of 20ml Herceptin diluent vials which is co-packaged with Herceptin® 440mg vials (batch number N3931B09). The reason for the recall is glass particulates were found in the reference samples of the diluent vials. |
| Recall action type: | Recall |
| Recall action: | Recall |
| Level of recall: | |
| Date Commenced: | 26/6/2020 |
