RecallRadar

FDA Device recall Z-1762-2017

iConnect Enterprise Archive (ICEA) software

On 2017-04-19 the FDA classified a Class II recall of iConnect Enterprise Archive (ICEA) software by Merge Healthcare, citing an error message can occur resulting in the prior studies being unavailable for viewing.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1762-2017
ClassificationClass II
Statusterminated
Initiated2016-04-04
Published2017-04-19
Last updated2026-09-13 11:54 UTC
CompanyMerge Healthcare
DistributionUS

Product

iConnect Enterprise Archive (ICEA) software. The firm name on the labeling is Merge Healthcare, Hartland, WI.

Reason

An error message can occur resulting in the prior studies being unavailable for viewing.

Identifiers

code_info
Versions : 8.30, 8.30.2, 8.40.0, 8.40.1, 8.40.1 HF0557, 8.40.s, 8.40.2.1, 8.40.2.2, 8.80, 8.80.0.1, 8.80.1.1, 8.80.2, 8…Versions : 8.30, 8.30.2, 8.40.0, 8.40.1, 8.40.1 HF0557, 8.40.s, 8.40.2.1, 8.40.2.2, 8.80, 8.80.0.1, 8.80.1.1, 8.80.2, 8.80.0.2, 9.0.0, 9.0.0.1, 9.1.0, 9.1.1, 9.1.2, 9.1.2.1, 9.1.2.2, 9.2.0, 9.3.0, 9.3.1, 9.4.0, 9.4.1, 9.4.2, 9.4.2.1., and 9.4.3

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-1762-2017%22

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