Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 37032 |
| Brand Name: | NextPhase Y connectors |
| Model: | Sontek Swivel Y Airway Connector |
| Affected: | Product code SMI-1002, SMI-1003 |
| Software version: | |
| Recalling Organisation: | Teleflex Medical New Zealand OFFICE 011, 110 CARLTON GORE ROAD Newmarket Auckland 1023 |
| Contact Information: | 027 476 4009 |
| Manufacturer: | NextPhase Medical Devices LLC |
| Issue: | The manufacturer is updating the Sontek Swivel Y Connector Instructions for Use (IFU) to incorporate an additional warning regarding catheter insertion. The revised IFU will advise users not to force the catheter through the seal when excessive resistance is encountered, in order to reduce the risk of device-related issues. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 7/7/2026 |
