IOLMASTER700 (2020-12-07)

Starting date:

December 7, 2020

Posting date:

December 24, 2020

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-74641

Last updated:
2020-12-24

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  Reason
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  Affected products

Affected Products 

IOLMASTER700

Reason

Based on post market surveillance activities, we found that the ZEISS IOLMaster 700 with software version 1.90.2.09 And 1.90.8.06, when used in conjunction with Modality Worklist (MWL) functionality, may not perform as expected. In rare cases this leads to a false display of patients in the patient manager screen.

Affected products