FDA Device Intelligence
HomeSONY CORPORATION › SONY

SONY

SONY CORPORATION · Model LMD-XH550T · UDI-DI 04548736132467

KQM Prescription
10
510(k) clearances
672
Adverse events
14
Recalls
195
Facilities

Description

LCD MONITOR

Recalls

DateFirmReason
2025-05-23Steris CorporationThis is a sub-recall of event RES 96885. The supplier identified that during their manufacturing process for a limited batch of MNA-6x0 (adapter) components the incorrect configura
2024-06-04Baxter Healthcare CorporationBaxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products l
2023-12-20Barco N.V.Barco became aware of a problem with I2C cables in the manufacturing process of a limited batch of MDSC-85xx NXF products. The functionality of the built-in MNA decoder is blocked
2015-05-28Barco Inc.User settings were no longer on the monitor's memory after these systems were powered off and back on.
2015-03-05Sony Latin AmericaMonitor has either not turned on or has lost image during clinical use.
2013-03-18Linvatec Corp. dba ConMed LinvatecThe VP1600 HD Still Capture Image System is recalled due to an anomaly between the software code in the VP1600 console and the communications interface for various keyboard key str
2010-10-25Mako Surgical CorporationMAKO Surgical Corporation recalled ONE infra-red camera MAKO PN 204854 which was a component of their RIO Robotic Arm Interactive Orthopedic System with SSN P7-03127, on November 2
2010-09-17Linvatec Corp. dba ConMed LinvatecIf the VHM Arm is left in the locked position, the gas spring can lose pressure and releasing the lock can result in a sudden downward movement.
2010-02-23Linvatec Corp. dba ConMed LinvatecConMed Linvatec, Endoscopy Division, dba. ConMed Linvatec, Largo, Florida is recalling five products: (1.) Video Cart Premium 120 VAC (VP6501), (2.) Video Cart Multi-Specialty 120
2010-02-23Linvatec Corp. dba ConMed LinvatecConMed Linvatec, Endoscopy Division, dba. ConMed Linvatec, Largo, Florida is recalling five products: (1.) Video Cart Premium 120 VAC (VP6501), (2.) Video Cart Multi-Specialty 120

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 docs
Data 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.