FDA Medical Device Recalls (openFDA)
Sony Medical Systems: Sony LMD-1951MD, Sony LMD1951MD/BS, Sony LMD-1951MC (Foreign) 19 inch medical grade liquid crystal display (LCD) Medical Monitors with light-emitting diode (LED) backlight technology.
- Recall number
- Z-2771-2015
- Recalling firm
- Sony Medical Systems
- Product
- Sony LMD-1951MD, Sony LMD1951MD/BS, Sony LMD-1951MC (Foreign) 19 inch medical grade liquid crystal display (LCD) Medical Monitors with light-emitting diode (LED) backlight technology.
- Status
- Terminated
- Initiated
- 2015-01-13
- Posted
- 2015-09-16
- Terminated
- 2017-04-26
- Reason
- Tthe medical monitor has either not turned on or has lost image during clinical use.
- Root cause
- Device Design
- Action
- Sony Corporation sent an URGENT: MEDICAL DEVICE FIELD ACTION field letter dated January 13, 2015. Customers are asked to affix the warning sticker to the rear of the monitor and place the adhesive seal over the AC inlet. If the firm does not possess an AC adaptor (AC-110MD) for each of the affected monitors, stop using the monitor and take the monitor out of service until the permanent corrective action described below is implemented.SEL will be replacing the power board of all affected units with a redesigned power board that does not exhibit the appropriate failure mode. Questions can be directed to 866-789-SONY (7669) between 8:00 am and 8:00 pm Monday through Friday.
- Quantity
- 4952 units (1016 US; 3936 OUS)
- Distribution
- Worldwide Distribution - US Distribution to the states of : AZ, CA, NC, PA, IA, OH and FL., and to the countries of : China, Japan, Taiwan, South Korea and Indonesia.
- Lot, serial or model codes
- Sony LMD-1951MD 3000038-3004884, 3100035-3100058, 3100065-3100145 Sony LMD-1951MC (Foreign) 5000001-5001925 5100001-5100157
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FWB
- Firm FEI
- 2246606
- Firm city
- Park Ridge
- Firm state
- NJ
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28