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

Recall Z-3214-2024 — GE Healthcare Centricty PACS, V2, V3, V4, V6, V7; Radiological imaging processing system.

U.S. FDA — Device Enforcement · United States · 2024-08-05 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-3214-2024
Date of alert
2024-08-05
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
GE Healthcare
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00840682124430
Reported risk: GE HealthCare has become aware of an issue where image storage is not possible when Centricity PACS reaches the maximum number of unique image identifiers (Ckeys). If this occurs, it can result in acquisition of a partial study.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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