FDA Device recall Z-0058-2013
Belmont Rapid Infuser, a Fluid Management System, Model FMS2000
- FDA Device
- Class II
- terminated
- Published 2012-10-24
On 2012-10-24 the FDA classified a Class II recall of Belmont Rapid Infuser, a Fluid Management System, Model FMS2000 by Belmont Instrument, citing leak from a saline bag caused saline to drip along the back of the Rapid infuser close to the Power Entry Module causing an electrical flash at the power entry area.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0058-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-09-25 |
| Published | 2012-10-24 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Belmont Instrument |
| Distribution | US |
Product
Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.
Reason
Leak from a saline bag caused saline to drip along the back of the Rapid infuser close to the Power Entry Module causing an electrical flash at the power entry area.
Identifiers
| code_info | Serial Numbers: 2012012793 2012012808 2012012809 2012022821 2012022822 2012022855 2012032880 2012032881 201203…Serial Numbers: 2012012793 2012012808 2012012809 2012022821 2012022822 2012022855 2012032880 2012032881 2012032883 2012032885 2012032886 2012032887 2012032888 2012032891 2012032904 2012032906 2012032907 2012032908 2012032910 2012042942 2012042944 2012052946 2012052948 2012052958 M030139 "1003 Q050656 Q050657" "2012012782 2012012783" "2012012784 2012012785" "2012012794 2012012795 2012012801 2012012802 2012012803 2012012805 2012022826" "2012012810 U082129" "2012022823 2012022824" "2012022827 2012022828" "2012022829 2012022830 2012022831 2012022832 2012022833 2012022834 2012022835" "2012022847 2012022848" "2012022849 2012022850 2012022851" "2012022852 2012022853" "2012032878 2012032879" "2012032881 2012032882 U011950 T121937" "2012032889 S121587" "2012032894 V092579" "2012032895 2012032902" "2012032903 U032005" "2012032908 2012032909 2012032911 2012042933" "2012052952 2012052954" J010005 J050006 J050008 |
|---|
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-0058-2013%22
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