Nextphase Y Connectors

Recalling firm
Teleflex Medical New Zealand
Product
NextPhase Y connectors. [Device]. Model: Sontek Swivel Y Airway Connector. Affected: Product code SMI-1002, SMI-1003
Reason
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.
Classification
Class I
Category
medical device recall
Country
New Zealand
Agency
MEDSAFE
Recall date
2026-07-07
Status
Ongoing
Distribution
New Zealand - Hospital/Pharmacy/Laboratory

Official recall notice from MEDSAFE

Recall details on Nibble Recalls: https://trynibble.app/recalls/b8499a47-74c1-4f04-92e4-2f61fa589e9e