FDA Device recall Z-2571-2014
V5Ms Transesophageal transducers
- FDA Device
- Class II
- terminated
- Published 2014-09-10
On 2014-09-10 the FDA classified a Class II recall of V5Ms Transesophageal transducers by Siemens Medical Solutions Usa, citing reports of deterioration of material covering the articulating section of the V5Ms transesophageal transducer.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2571-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-08-13 |
| Published | 2014-09-10 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
V5Ms Transesophageal transducers; V5Ms trans-esophageal echocardiograph (TEE) ultrasound transducer is intended primarily for cardiology applications
Reason
Reports of deterioration of material covering the articulating section of the V5Ms transesophageal transducer.
Identifiers
| code_info | Model numbers 8264577 and 8263703; Serial numbers: US: 33707625 32807460 34507747 42208166 S34707777 32907477…Model numbers 8264577 and 8263703; Serial numbers: US: 33707625 32807460 34507747 42208166 S34707777 32907477 33007494 33307538 33507577 33507584 33707612 34107671 34707781 40908018 41508085 41608100 41908126 41908129 S34607757 S34907818 33907638 33907642 34807802 33007497 34207690 34307704 34607760 40607983 41808117 41908127 35107862 35107863 40107882 40407947 S34307696 33707631 34207694 33007487 41508082 41608089 34707771 41708101 33207509 33207519 33207522 33707622 34907824 35107872 40107896 42008137 33207520 41708109 S34607755 33307537 33607596 33707619 34607768 41808119 33707630 42008136 40407946 34207680 34607762 40808002 41008037 41708108 S33207505 33507578 41108046 41308062 42008132 34307703 34707778 40307937 40407951 40808007 41908128 40207906 32907474 33307539 34607758 35107875 40908017 41308054 41508088 41508080 41508087 33507576 33607590 33707621 40407958 40607982 41008032 418081 |
|---|
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-2571-2014%22
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