Centricity PACS Web Diagnostic — Class II medical device recall Z-1782-2017
Terminated recall by Ge Medical Systems Information T, reported 2017-04-19, distributed nationwide. It was reported from a complaint that study category labels of "Prior" and "Baseline" and hanging position app
| Recall number | Z-1782-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ge Medical Systems Information T, Barrington, IL, United States |
| Recall initiated | 2013-02-18 |
| Classified | 2017-04-11 |
| Reported by FDA | 2017-04-19 |
| Terminated | 2017-07-31 |
| Distributed | Nationwide (US) |
| Quantity | 118 |
| Reason classes | labeling |
Product
Centricity PACS Web Diagnostic (WebDX) by GE Healthcare Dynamic Imaging Solutions is a device that receives medical images (including mammograms) and data from various imaging sources within the system or across computer networks at distributed locations.
Reason for recall
It was reported from a complaint that study category labels of "Prior" and "Baseline" and hanging position appeared incorrectly swapped when the hanging protocol for three comparison studies is manually applied from the patient folder.
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-1782-2017. 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.