iConnect Enterprise Archive — Class II medical device recall Z-1762-2017
Terminated recall by Merge Healthcare, Inc., reported 2017-04-19, distributed nationwide. An error message can occur resulting in the prior studies being unavailable for viewing.
| Recall number | Z-1762-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Merge Healthcare, Inc., Hartland, WI, United States |
| Recall initiated | 2016-04-04 |
| Classified | 2017-04-07 |
| Reported by FDA | 2017-04-19 |
| Terminated | 2020-06-15 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 333 sites |
Product
iConnect Enterprise Archive (ICEA) software. The firm name on the labeling is Merge Healthcare, Hartland, WI.
Reason for recall
An error message can occur resulting in the prior studies being unavailable for viewing.
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-1762-2017. 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.