Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:15709
Brand Name:GE Patient Data Module (PDM)
Model:Product Codes: SA3 and SG5
Affected:Manufactured between Apr-2007 and Dec-2012
Software version:
Recalling Organisation:GE Healthcare Limited
Level 7, Vero Centre
48 Shortland St
Auckland 1010
Contact Information:0800 659 465
Manufacturer:GE Medical Systems Information Technologies Inc
Issue:The spring inside the mounting latch can become dislodged causing the PDM not to latch properly resulting in an unexpected loss of patient monitoring function. This may also result in the PDM falling onto a patient or caregiver.
Recall action type:Correction
Recall action:Product to be modified
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:22/11/2013
Hide menus
Show menus
0 1 2 4 5 6 7 9 [ /