FDA Device recall Z-1133-2013
GE Healthcare Muse v7 cardiology information system
- FDA Device
- Class II
- terminated
- Published 2013-04-24
On 2013-04-24 the FDA classified a Class II recall of GE Healthcare Muse v7 cardiology information system by Ge Healthcare, citing GE Healthcare conducted a recall on the Muse v7 because incorrect medications were displayed on the MUSE, which could result in incorrect treatment.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1133-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-01-04 |
| Published | 2013-04-24 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Ge Healthcare |
| Distribution | US |
Product
GE Healthcare Muse v7 cardiology information system. Model number 2026443-001: MUSE 7.0 app cd, Model Number 2026443-015: MUSE 7.0.2 app cd, Model number 2026443-017: MUSE 7.1 app cd, Model number 2026443-029:MUSE 7.1.1 A app cd, and Model Number 2026443-031: MUSE 7.1.1 app cd. Intended to store, access and manage cardiovascular information on adult and pediatrics patients.
Reason
GE Healthcare conducted a recall on the Muse v7 because incorrect medications were displayed on the MUSE, which could result in incorrect treatment.
Identifiers
| code_info | Serial Number SBP05450003GA SBP05450009GA SBP05500067GA SBP06100195GA SBP06110200GA SBP06110203GA SBP06160274GA…Serial Number SBP05450003GA SBP05450009GA SBP05500067GA SBP06100195GA SBP06110200GA SBP06110203GA SBP06160274GA SBP06170288GA SBP06180296GA SBP06180306GA SBP06180308GA SBP06190316GA SBP06190326GA SBP06190329GA SBP06190330GA SBP06200371GA SBP06200377GA SBP06230507GA SBP06230512GA SBP06250577GA SBP06260614GA SBP06260619GA SBP06280624GA SBP06280626GA SBP06280629GA SBP06280637GA SBP06280653GA SBP06290744GA SBP06290748GA SBP06290758GA SBP06290768GA SBP06300778GA SBP06300789GA SBP06310812GA SBP06310814GA SBP06330820GA SBP06330824GA SBP06330838GA SBP06330841GA SBP06330853GA SBP06330873GA SBP06330878GA SBP06340958GA SBP06340959GA SBP06360974GA SBP06360979GA SBP06360983GA SBP06361019GA SBP06371040GA SBP06371055GA SBP06371058GA SBP06371061GA SBP06391095GA SBP06391100GA SBP06411137GA SBP06411147GA SBP06421164GA SBP06421167GA SBP06421169GA SBP06421171GA SBP06421183GA SBP06421189GA SBP06431228GA SBP06441246GA SBP06441251GA SBP0644127 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1133-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.