Home › LG Electronics Inc. › LG
LG
LG Electronics Inc. · Model 27HJ710S · UDI-DI 00719192609198
FWB
Prescription
6
510(k) clearances
173
Adverse events
2
Recalls
35
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-12-15 | Trumpf Medical Systems, Inc. | 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 r |
| 2015-01-13 | Sony Medical Systems | Tthe medical monitor has either not turned on or has lost image during clinical use. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.