Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 22833 |
| Brand Name: | Teleflex Medical RTP - Valve, non-rebreathing |
| Model: | |
| Affected: | Affected lot numbers 74D1501706, 74K1502092, 74F1600367, 74J1600117, 74L1601916, 74C1701733, 74F1700707, 74D1501731, 74K1502045, 74F1601072, 74J1601101, 74M1600284, 74C1702365, 74F1701866 |
| Software version: | |
| Recalling Organisation: | Teleflex Medical New Zealand OFFICE 011, 110 CARLTON GORE ROAD Newmarket Auckland 1023 |
| Contact Information: | 027 476 4009 |
| Manufacturer: | Teleflex Medical Inc |
| Issue: | The manufacturer has indentified that the HUDSON RCI One-Way Valve with Capped may disconnect at the joint between the two components that make up the device, which would cause an interruption of ventilation to the patient. Disconnection of the valve is recognizable by the user as an alarm from the ventilator, oxygen sensor or other compatible device to which the valve is connected. However, disconnection of the valve in ventilator dependent patients without prompt response could lead to hypoxia, organ failure, or death |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 19/4/2018 |
