Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Medicine |
| Medsafe Reference: | 22549 |
| Brand Name: | Lodi |
| Dose Form/Strength: | Concentrate for infusion 50 mg/mL |
| Affected: | |
| Recalling Organisation: | REX Medical Ltd Unit 18/273 Neilson Street Onehunga Auckland 1061 |
| Contact Information: | |
| Manufacturer: | Bioindustria Laboratorio Medicinali SpA |
| Issue: | Notification received from BOPDHB that St John has identified what appears to be glass in certain ampoules from a batch of this product. From the email chain forwarded to Medsafe, it appears that ADHB has identified a similar issue across multiple batches of this product. |
| Recall action type: | Communication to healthcare professionals |
| Recall action: | Product alert |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 7/2/2018 |
