CLASS II Device recall · Reported 29 Apr 2015 · FDA Enforcement Report
Sony Medical Monitor LMD-1951MD recalled by Sony Latin America
Sony Latin America is recalling Sony Medical Monitor LMD-1951MD, distributed in Florida, North Carolina. The recall was initiated on 5 Mar 2015 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1514-2015
- FDA event ID
- 70702
- Recalling firm
- Sony Latin America, Miami, FL
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 5 Mar 2015
- FDA classified
- 23 Apr 2015
- Reported
- 29 Apr 2015
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Other Reasons
- Device type
- Patient Monitors
Timeline
| 5 Mar 2015 | Recall initiated by company | |
| 23 Apr 2015 | Classified by FDA | +49 days |
| 29 Apr 2015 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Monitor has either not turned on or has lost image during clinical use.
Product as listed by the FDA
Sony Medical Monitor LMD-1951MD 19 inch
Where it was distributed
Worldwide Distribution - US Distribution to the states of : FL and NC., and to the countries of : Ecuador, Costa Rica, Brazil, Nicaragua, Venezuela, Peru, Colombia, Dominican Republic, and South Korea.
Questions about this recall
Why was it recalled?
Monitor has either not turned on or has lost image during clinical use.
Which lots are affected?
Serial number range: 3000038-3004884, 3100035-3100058, 3100065-3100145.
Where was it sold?
Worldwide Distribution - US Distribution to the states of : FL and NC., and to the countries of : Ecuador, Costa Rica, Brazil, Nicaragua, Venezuela, Peru, Colombia, Dominican Republic, and South Korea.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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