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Recall Observatory FDA recall evidence

Device product

Imagecast PACS with Centricity RIS-IC versions prior to 10.6 Update Package 18 Product Usage: is an image management system intended to be used by trained professionals, including but not limited to physicians, nurses and medical technicians. The system is used with general purpose computing hardware to acquire, transmit, process and store images and data throughout a clinical environment. Data and images are acquired through DICOM compliant imaging devices and modalities. Lossy compressed mammographic images and digitized film screen images must not be reviewed for primary image interpretation. Mammographic images may only be interpreted using an FDA approved monitor that offers at least 5 Mpixel resolution and meets other technical specifications reviewed and accepted by the FDA.

Z-2300-2016

February 18, 2013

Class II

Product summary

Firm
Ge Healthcare It
Event
Event 64758
Status
Terminated
Classification
Class II
Quantity
13
Official record key
device-enforcement:Z-2300-2016

Official wording

Reason: A software defect was discovered that causes images to be out of context with clinical information.

Code information: Imagecast PACS 3.5.69, 3.5.86, 3.5.87 and 3.6 with Centricity. RIS-IC 10.6 versions prior to update Package 18.

Distribution pattern: US Nationwide Distribution.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software defect