GE Healthcare, LLC GE Centricity Universal Viewer Zero Footprint Client Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
GE Centricity Universal Viewer Zero Footprint Client
Brand
GE Healthcare, LLC
Lot Codes / Batch Numbers
Versions 6.0 SP9, SP9.0.1, SP9.0.1.1, SP9.0.1.2, SP9.0.1.3, SP9.0.1.4, SP9.0.1.5, SP10, SP10.1, SP10.2, SP10.2.1, SP10.2.1.1, SP10.2.2, SP10.2.2.1 configured with a Centricity PACS back end. GTIN 00840682102988, UDI 00840682102988.
Products Sold
Versions 6.0 SP9, SP9.0.1, SP9.0.1.1, SP9.0.1.2, SP9.0.1.3, SP9.0.1.4, SP9.0.1.5, SP10, SP10.1, SP10.2, SP10.2.1, SP10.2.1.1, SP10.2.2, SP10.2.2.1 configured with a Centricity PACS back end. GTIN 00840682102988; UDI 00840682102988.
GE Healthcare, LLC is recalling GE Centricity Universal Viewer Zero Footprint Client due to There is a potential to display incomplete patient imaging study.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
There is a potential to display incomplete patient imaging study.
Recommended Action
Per FDA guidance
The firm issued medical device correction letters dated 10/15/2021 on the same date via traceable means. The letter described the safety issue and actions to be taken. The letter informed the consignee they can continue to use the device by following the instructions provided in the letter until a GE Service Representative can restart their ZFP system.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026