Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Medicine |
| Medsafe Reference: | 16576 |
| Brand Name: | Xyntha |
| Dose Form/Strength: | Injection with diluent 500 IU |
| Affected: | H19478 |
| Recalling Organisation: | Pfizer New Zealand Limited C/-ICON Clinical Research New Zealand Ltd Plaza Level, c/-Regus 41 Shortland Street AUCKLAND 1010 |
| Contact Information: | 0800 734 076 |
| Manufacturer: | Wyeth Farma SA |
| Issue: | Complaint received regarding incorrect labelling. The dual chamber syringe was labelled as Refacto 3000IU and the outer packaging was labelled correctly as Xyntha 500IU. |
| Recall action type: | Recall |
| Recall action: | Recall |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 5/6/2014 |
