Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 19941 |
| Brand Name: | Simtomax In vitro screening test for Coeliac Disease |
| Model: | |
| Affected: | Batches: 192065, 195218, 195220 and 195378 |
| Software version: | |
| Recalling Organisation: | Smith Biomed (NZ) Ltd Level 2 44B Victoria Road New Plymouth |
| Contact Information: | |
| Manufacturer: | Augurix SA |
| Issue: | Due to an issue with over labelling of the Simtomax Coeliac disease test the expiry dates may not correctly match the stock supplied. The efficacy of the test is not in question however stock received may not necessarily reflect the correct batch that should have been received. The tests are not past their expiry date and the tests that consumers have taken to date had not expired and the efficacy of the test is not in question. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Wholesale |
| Date Commenced: | 29/3/2016 |
