Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:37723
Brand Name:Intuitive Surgical - Robotic forceps
Model:
Affected:Affected Product: 470033, 470036, 470048, 470093, 470181, 470190, 470347, 471048, 471190
Software version:
Recalling Organisation:Device Technologies New Zealand
47 Arrenway Drive
Albany
AUCKLAND 0632
Contact Information:09 913 2000
Manufacturer:Intuitive Surgical Inc
Brand Name:Intuitive Surgical - Bipolar instruments
Model:Affected Product: 470171, 470344, 471171, 471344, 471405
Affected:
Software version:
Recalling Organisation:Device Technologies New Zealand
47 Arrenway Drive
Albany
AUCKLAND 0632
Contact Information:09 913 2000
Manufacturer:Intuitive Surgical Inc
Brand Name:Intuitive Surgical - Clip applier
Model:Affected Product: 470401, 470230, 470327
Affected:
Software version:
Recalling Organisation:Device Technologies New Zealand
47 Arrenway Drive
Albany
AUCKLAND 0632
Contact Information:09 913 2000
Manufacturer:Intuitive Surgical Inc
Brand Name:Intuitive Surgical - Needle driver
Model:Affected Product: 470194, 470309, 471296, 471309
Affected:
Software version:
Recalling Organisation:Device Technologies New Zealand
47 Arrenway Drive
Albany
AUCKLAND 0632
Contact Information:09 913 2000
Manufacturer:Intuitive Surgical Inc
Brand Name:Intuitive Surgical - Robotic scissors
Model:Affected Product: 470001, 470007
Affected:
Software version:
Recalling Organisation:Device Technologies New Zealand
47 Arrenway Drive
Albany
AUCKLAND 0632
Contact Information:09 913 2000
Manufacturer:Intuitive Surgical Inc
Brand Name:Intuitive Surgical - Retractor
Model:Affected Product: 470246, 470249
Affected:
Software version:
Recalling Organisation:Device Technologies New Zealand
47 Arrenway Drive
Albany
AUCKLAND 0632
Contact Information:09 913 2000
Manufacturer:Intuitive Surgical Inc
Issue:The grip cables that control the opening and closing of the jaws of the instrument can fail partially (i.e. frayed) or completely (i.e. broken). A broken grip cable can lead to loss of grip functionality, exposure to frayed cables, or the potential for tungsten cable particulate to fall into the patient. If a cable were to fail, it would be retained within the shaft of the instrument. As a result, fragments would not fall into the patient, though particulate may be generated. A partial failure might not affect grip functionality but may lead to exposure to frayed cables.
As part of a comprehensive review and ongoing evaluation, the manufacturer identified a total of six additional reusable instruments with jaws with increased complaint rates. Four of these devices were part of the August 2025 recall (Medsafe Ref #34521).
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:15/10/2026
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