FDA Device recall Z-2159-2016
Merge OfficePACS software
- FDA Device
- Class II
- terminated
- Published 2016-07-20
On 2016-07-20 the FDA classified a Class II recall of Merge OfficePACS software by Merge Healthcare, citing potential data loss occurs as a result of product archiving not working properly.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2159-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-01-31 |
| Published | 2016-07-20 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Merge Healthcare |
| Distribution | AL, AZ, CA, CO, CT, FL, GA, ID, IL, KY, MA, MO, NC, NE, NH, NJ, NY, OK, PA, SC, TN, VA, WA |
Product
Merge OfficePACS software. The firm name on the label is Merge Healthcare, Heartland, WI.
Reason
Potential data loss occurs as a result of product archiving not working properly.
Identifiers
| code_info | Version 3.4 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2159-2016%22
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