Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:21568
Brand Name: CS - Adaptor, luer (DLP)
Model:
Affected: DLP Extension Line Adapters 20 in length, DLP Antegrade/Retrograde Adapter, DLP Cardioplegia Adapter with Pressure Port, Multiple Lots
Software version:
Recalling Organisation:Medtronic New Zealand Limited
Unit 16 Mezzanine Level
5 Gloucester Park Road
Onehunga
AUCKLAND
Contact Information:0800 377 807
Manufacturer:Medtronic Inc
Brand Name:CS - Tubing set, pressure monitoring, invasive blood pressure
Model:
Affected:DLP Pressure Monitoring Extension Line Adapters, DLP Pressure Disposable Pressure Display Sets , Multiple Lots
Software version:
Recalling Organisation:Medtronic New Zealand Limited
Unit 16 Mezzanine Level
5 Gloucester Park Road
Onehunga
AUCKLAND
Contact Information:0800 377 807
Manufacturer:Medtronic Inc
Issue:During the manufacturing process, the manufacturer identified small pinholes, approximately 1 mm or less in diameter, in a single packaging configuration of sterile pouches. Based on internal investigation, all products in this packaging configuration manufactured since March 1, 2016 are potentially affected. The result is a potential sterile barrier breach.
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:21/6/2017
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