Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:21355
Brand Name:Infusion pumps - Syringe (Swiss)
Model:
Affected:Product codes with prefix (all variants): 8001, 8002, 8003, 8004, 8005
Software version:
Recalling Organisation:CareFusion New Zealand 313 Limited
Unit 4 / 110 Mays Road
Onehunga
AUCKLAND 1061
Contact Information:0508 422 734
Manufacturer:CareFusion Switzerland 317 Sarl
Issue:The manufacturer has identified that a breakage of the plunger backplate spring may allow movement of the syringe plunger within the plunger holder mechanism; this may result in siphonage. In some circumstances, this may result in a clinically significant over infusion.
Recall action type:Correction
Recall action:Product to be modified
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:27/4/2017
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