Drug recall
Centricity Enterprise Archive V2, V3, and V4, software product for receiving, archiving, and sending…
FDA recall event 99661 · Class II · GE Healthcare
Key facts
| Event ID | 99661 |
|---|---|
| Recall numbers | Z-3166-2026, Z-3167-2026, Z-3168-2026, Z-3169-2026, Z-3170-2026, Z-3171-2026 |
| Recalling firm | GE Healthcare |
| Product type | Devices |
| Products | Centricity Enterprise Archive V2, V3, and V4, software product for receiving, archiving, and sending electronic medical data, All Versions, Centricity PACS Server V7, intended for managing digital medical images and associated data, All versions, Centricity PACS V2, V3, V4, V6, V7, software product is intended for the storage, reading, diagnostic review, analysis, annotation, distribution, printing, editing, and processing of digital images…, Core Services Hub V8, a set of backend services including Cross Enterprise (XE) and Workflow Core (WFC) services that enables enterprise imaging workflows, All versions, Enterprise Archive V8, software product for receiving, archiving, and sending electronic medical data, All versions and 1 more |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the… |
| Initiation date | Jul 31, 2026 |
| Report date | Sep 23, 2026 |
| City | Chicago |
| State | IL |
| Country | United States |
| FEI number | 3004526608 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: