Merge PACS — Class II medical device recall Z-2944-2020
Terminated recall by Merge Healthcare, Inc., reported 2020-09-16, distributed in AR, CA, CT, DE, FL, GA, IL, IN…. Measurements done on the Merge PACS generated MPR s may have incorrect measurements.
| Recall number | Z-2944-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Merge Healthcare, Inc., Hartland, WI, United States |
| Recall initiated | 2020-08-06 |
| Classified | 2020-09-09 |
| Reported by FDA | 2020-09-16 |
| Terminated | 2022-11-30 |
| Distributed | AR, CA, CT, DE, FL, GA, IL, IN, MD, MI, MN, MO, MS, NC, ND, NE, NH, NM, NY, OH, SC, TX, UT, VA, WI |
| Countries outside the US | GB |
| Quantity | 125 units |
| UPC / GTIN / UDI-DI | 00842000100805 |
Product
Merge PACS
Reason for recall
Measurements done on the Merge PACS generated MPR s may have incorrect measurements.
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-2944-2020. 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.