Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1302-2018 — GE Healthcare Centricity PACS-IW, Model Numbers: (a) 2052831-00X (b) 2049588-008 Product Usage: Centricity PACS-IW by GE Healthcare is a device that receives medical images (including mammograms) and data from various imaging sources. Images and data can be stored, communicated, processed and

U.S. FDA — Device Enforcement · United States · 2018-02-23 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1302-2018
Date of alert
2018-02-23
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
GE Healthcare
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00558123
Reported risk: A database handling error could occur during the image acquisition process affecting the completeness of acquired images with Centricity PACS-IW. There is a potential that one or more image series (i.e. all images within an image set) may be missing from an exam without indication to the user. While this is rare, this can occur with imaging studies that consist of a very small number of images per series. E.g. CR Thorax exam with 1 image per series.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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