FDA Device recall Z-0824-2018
Camera System, Television, Surgical without audio Intended for transmission and documentation of surgical interventions for the purpose of…
- FDA Device
- Class II
- terminated
- Published 2018-03-07
On 2018-03-07 the FDA classified a Class II recall of Camera System, Television, Surgical without audio Intended for transmission and documentation of surgical interventions for the purpose of… by Trumpf Medical Systems, citing the radiated emission from the TruVidia" Wireless Receiver is above the normative accepted limits, in which the radiated emission may interact with other devices in the operating….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0824-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-12-15 |
| Published | 2018-03-07 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Trumpf Medical Systems |
| Distribution | GA, IL, IN, PA, SC, TX, UT, VA |
Product
Camera System, Television, Surgical without audio Intended for transmission and documentation of surgical interventions for the purpose of archiving and teaching.
Reason
The radiated emission from the TruVidia" Wireless Receiver is above the normative accepted limits, in which the radiated emission may interact with other devices in the operating room and cause them not to function properly.
Identifiers
| code_info | Catalog Number 1940747, All serial numbers: 102584474, 102584475, 102584477, 102584478, 102805330, 102813656, 102813657…Catalog Number 1940747, All serial numbers: 102584474, 102584475, 102584477, 102584478, 102805330, 102813656, 102813657, 102813658, 102813659, 102813660, 102813661, 102813662, 102860647, 102860652, 102863706, 102863707, 102867783, 102867784, 102925734, 102925735, 102925736, 102925737, 102925738, 102925739, 102925740, 102925741, 102925742, 102925743, 102928703, 102932185, 102932186, 102932187, 102932188, 102932189, 102932203, 102932204, 102932205, 102932206, 102932207, 102932208, 102932209, 102932210, 102932211, 102932212, 102932217, 102932218, 102932219, 102932220, 102932221, 102932223, 102934525, 102934526, 102934527, 102934528, 102934529, 102936117, 102939484, 102940382, 102940383, 102940384, 102940386, 102940387, 102940388, 102940389, 102940390, 102940391, 102940408, 102940409, 102940410, 102961390, 102961391, 102961392, 102961393, 102961394, 102961395, 102961396, 102961397, 102961398, 102961399, 102961400, 102961401, 102975336, 102986494, 102986495, 102988480, 102989096, 102989607, |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Other recalls by Trumpf Medical Systems
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FDA Device · Class II · 2016-11-16 · Trumpf Medical Systems - Stationary Column TruSystem 7599, Material Number 1717020 Patient positioning during surgery, ranging from anesthesia induction to actual s…
FDA Device · Class II · 2016-10-12 · Trumpf Medical Systems - Mobile Column TruSystem 7500, Material Number 1717023
FDA Device · Class II · 2016-10-12 · Trumpf Medical Systems - Operating Table TruSystem 7000 U, Material Number 1604788
FDA Device · Class II · 2016-10-12 · Trumpf Medical Systems - Floor Mounting Column TS 7500 U, Material Number 1730732
FDA Device · Class II · 2016-10-12 · Trumpf Medical Systems
All Trumpf Medical Systems recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0824-2018%22
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