Centricity PACS-IW — Class II medical device recall Z-1502-2023
Ongoing recall by GE Healthcare, reported 2023-05-10. GE HealthCare has become aware of an issue where information from two different patients can be mismatched whe
| Recall number | Z-1502-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Healthcare, Chicago, IL, United States |
| Recall initiated | 2023-03-28 |
| Classified | 2023-05-02 |
| Reported by FDA | 2023-05-10 |
| Quantity | 153 units |
Product
Centricity PACS-IW, Product ID Numbers: a) 2041037-001, b) 2042988-001, c) 2049587-009, d) 2049587-011, e) 2049587-012, f) 2049587-015, g) 2052829-001, h) Not applicable; Radiological Image Processing System
Reason for recall
GE HealthCare has become aware of an issue where information from two different patients can be mismatched when correcting patient or study information.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1502-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.