Database updated: 24 October 2025
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 21840 |
| Brand Name: | Bayer Essure |
| Model: | |
| Affected: | ESS305 All Batch numbers |
| Software version: | |
| Recalling Organisation: | New Zealand Medical & Scientific Ltd 2A Fisher Crescent Mt Wellington AUCKLAND 1060 |
| Contact Information: | 09 259 4062 |
| Manufacturer: | Bayer AG |
| Issue: | Unimplanted product is being recalled as the CE mark has been temporarily suspended. Physicians are being informed of possible adverse events following implantation and being requested to monitor patients. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 8/9/2017 |
