RecallRadar

FDA Device recall Z-0773-2014

Imagecast PACS is an image management system intended to be used by trained professionals, including but not limited to physicians, nurses…

On 2014-01-22 the FDA classified a Class II recall of Imagecast PACS is an image management system intended to be used by trained professionals, including but not limited to physicians, nurses… by Ge Healthcare It, citing in Imagecast PACS versions prior to 3.6.51.01, the estimated magnification factor (0018,1114) was not accounted for. These versions of Imagecast PACS look for values to be present….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0773-2014
ClassificationClass II
Statusterminated
Initiated2011-03-04
Published2014-01-22
Last updated2026-09-13 11:53 UTC
CompanyGe Healthcare It
DistributionUS

Product

Imagecast PACS 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 and interpretations. Mammongraphic 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.

Reason

In Imagecast PACS versions prior to 3.6.51.01, the estimated magnification factor (0018,1114) was not accounted for. These versions of Imagecast PACS look for values to be present in the following tags to calculate a measurement from pixels to millimeters (mm): (0020,0030) Pixel Spacing and, (0018,1164) Imager Pixel Spacing. Because the estimated magnification factor is not used, distance meas

Identifiers

code_infoImagecast PACS versions prior to 3.6.51.01

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0773-2014%22

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