Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Medicine |
| Medsafe Reference: | 19207 |
| Brand Name: | Morphine 300mcg/0.3ml intrathecal syringe - compounded product |
| Dose Form/Strength: | |
| Affected: | Batches 29946, and 29947 |
| Recalling Organisation: | Biomed Limited 52 Carrington Road Point Chevalier AUCKLAND |
| Contact Information: | 0800 833 133 |
| Manufacturer: | Biomed Limited |
| Brand Name: | Morphine 200mcg/0.4ml intrathecal syringe - compounded product |
| Dose Form/Strength: | |
| Affected: | Batches 29941, 29942, 29943, 29944, 29945, 29951 and 29952 |
| Recalling Organisation: | Biomed Limited 52 Carrington Road Point Chevalier AUCKLAND |
| Contact Information: | 0800 833 133 |
| Manufacturer: | Biomed Limited |
| Brand Name: | Fentanyl 20mcg/0.4ml intrathecal syringe - compounded product |
| Dose Form/Strength: | |
| Affected: | Batch 29948 |
| Recalling Organisation: | Biomed Limited 52 Carrington Road Point Chevalier AUCKLAND |
| Contact Information: | 0800 833 133 |
| Manufacturer: | Biomed Limited |
| Issue: | Notification of a contamination issue in a compounded intrathecal syringe containing Morphine 300 mcg/0.3ml. The contaminant was found inside the syringe cap (brown spots), syringe tip (brown flecking) and inside the syringe nozzle (brown spot). |
| Recall action type: | Recall |
| Recall action: | Recall |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 1/10/2015 |
