Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Medicine |
| Medsafe Reference: | 26923 |
| Brand Name: | Largactil |
| Dose Form/Strength: | Solution for injection 25 mg/mL |
| Affected: | A90141 |
| Recalling Organisation: | Sanofi-Aventis New Zealand Limited Level 8 56 Cawley Street Ellerslie AUCKLAND 1051 |
| Contact Information: | 0800 283 684 |
| Manufacturer: | Sanofi SRL |
| Issue: | Sanofi-aventis new zealand limited is recalling one batch (A90141) of LARGACTIL chlorpromazine hydrochloride 50mg/2mL injections due to oxidation of a small number of ampoules during manufacture. |
| Recall action type: | Recall |
| Recall action: | Recall |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 27/11/2020 |
