Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:18809
Brand Name:Teleflex Hudson RCI Lifesaver Single Patient Use Manual Resuscitator
Model:5362
Affected:Manufactured between Jun-2014 and Apr-2015
Software version:
Recalling Organisation:Ebos Group Ltd
108 Wrights Road
Addington
Christchurch
Contact Information:0800 18 17 16
Manufacturer:Galemed Corporation
Issue:The oxygen intake port may be blocked which can prevent the bag from filling. This may prevent the device from delivering breathing support to the patient. A delay in treatment may potentially lead to patient injury or death. To date, Teleflex has not received any reports of patient injury or death related to this issue.
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Healthcare Professional
Date Commenced:8/7/2015
Hide menus
Show menus
0 1 2 4 5 6 7 9 [ /