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Medical Device

Workflow Core Services V8, intended to provide set of services for storage and retrieval of patient data, exams and performs system Administ

Recall date: 2026-09-23 · Source: FDA_DEVICE
Brand / Firm
Product
Workflow Core Services V8, intended to provide set of services for storage and retrieval of patient data, exams and performs system Administration, common configuration management for consuming applications, All versions
Reason for recall
Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record, which could lead to misdiagnosis or a delay in patient care.
Units affected
169 systems
Description
Workflow Core Services V8, intended to provide set of services for storage and retrieval of patient data, exams and performs system Administration, common configuration management for consuming applications, All versions
View official recall notice →