Drug recall
Camera System, Television, Surgical without audio Intended for transmission and documentation of surgical…
FDA recall event 79336 · Class II · Trumpf Medical Systems, Inc.
Key facts
| Event ID | 79336 |
|---|---|
| Recall numbers | Z-0824-2018 |
| Recalling firm | Trumpf Medical Systems, Inc. |
| Product type | Devices |
| Products | Camera System, Television, Surgical without audio Intended for transmission and documentation of surgical interventions for the purpose of archiving and teaching. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | 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… |
| Initiation date | Dec 15, 2017 |
| Report date | Mar 7, 2018 |
| Termination date | Apr 23, 2020 |
| City | Charleston |
| State | SC |
| Country | United States |
| FEI number | 3003184737 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: