Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 28764 |
| Brand Name: | Imigran Autoinjector |
| Model: | |
| Affected: | User leaflet update, GH9K, 9F4J. |
| Software version: | |
| Recalling Organisation: | GlaxoSmithKline NZ Limited Aon Centre Level 12/29 Customs Street West Auckland CBD Auckland 1010 |
| Contact Information: | (09) 367 2914 |
| Manufacturer: | Glaxo Operations UK Ltd |
| Issue: | The manufacturer has identified an error in an image in the User Leaflet pack insert for Imigran Auto-Injector medical device. The image at Step 4 of the User Leaflet incorrectly suggests that after loading the autoinjector (pen) a syringe needle is visible. The needle is visible only after the injection is given. The written instructions adjacent to the image are correct. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Healthcare Professional |
| Date Commenced: | 11/1/2022 |
