Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:29285
Brand Name:KARL STORZ Flexible Endoscopes 44715-IIa
Model:
Affected:IFU update Certain KARL STORZ Flexible Endoscopes
Software version:
Recalling Organisation:KARL STORZ Endoscopy New Zealand Limited
31 Morningside Drive
Mt Albert
AUCKLAND 1025
Contact Information:
Manufacturer:Karl Storz SE & Co KG
Brand Name:KARL STORZ Flexible Endoscopes37181-IIa
Model:
Affected:IFU update Certain KARL STORZ Flexible Endoscopes
Software version:
Recalling Organisation:KARL STORZ Endoscopy New Zealand Limited
31 Morningside Drive
Mt Albert
AUCKLAND 1025
Contact Information:
Manufacturer:Karl Storz SE & Co KG
Brand Name:KARL STORZ Flexible Endoscopes 36632-IIa
Model:
Affected:IFU update Certain KARL STORZ Flexible Endoscopes
Software version:
Recalling Organisation:KARL STORZ Endoscopy New Zealand Limited
31 Morningside Drive
Mt Albert
AUCKLAND 1025
Contact Information:
Manufacturer:Karl Storz SE & Co KG
Brand Name: KARL STORZ Flexible Endoscopes 44925-IIa
Model:
Affected:IFU update Certain KARL STORZ Flexible Endoscopes
Software version:
Recalling Organisation:KARL STORZ Endoscopy New Zealand Limited
31 Morningside Drive
Mt Albert
AUCKLAND 1025
Contact Information:
Manufacturer:Karl Storz SE & Co KG
Brand Name:KARL STORZ Flexible Endoscopes 37111-IIa
Model:
Affected:IFU update Certain KARL STORZ Flexible Endoscopes
Software version:
Recalling Organisation:KARL STORZ Endoscopy New Zealand Limited
31 Morningside Drive
Mt Albert
AUCKLAND 1025
Contact Information:
Manufacturer:Karl Storz SE & Co KG
Brand Name:KARL STORZ Flexible Endoscopes34939-IIa
Model:
Affected:IFU update Certain KARL STORZ Flexible Endoscopes
Software version:
Recalling Organisation:KARL STORZ Endoscopy New Zealand Limited
31 Morningside Drive
Mt Albert
AUCKLAND 1025
Contact Information:
Manufacturer:Karl Storz SE & Co KG
Brand Name:KARL STORZ Flexible Endoscopes38703-IIa
Model:
Affected:IFU update Certain KARL STORZ Flexible Endoscopes
Software version:
Recalling Organisation:KARL STORZ Endoscopy New Zealand Limited
31 Morningside Drive
Mt Albert
AUCKLAND 1025
Contact Information:
Manufacturer:Karl Storz SE & Co KG
Issue:The correction is limited to a labeling update to correct the Instructions for Use for certain flexible endoscopes and advise that CIDEX OPA should not be used for manual high-level disinfection.
Recall action type:Correction
Recall action:Instructions for use to be updated
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:20/4/2022
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