NA EX2721, TM220Recalls & reported problems
Eizo Corporation · 27-inch Full HD monitor · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04995047053118), received between Aug 30, 2023 and Aug 30, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 30, 2023Insufficient Device Problem Information; Insufficient Device Problem Information
ON 30-JAN 2023, EIZO CORPORATION RECEIVED AN INCIDENT REPORT FROM KARL STORZ SE & CO. KG, A LAPAROSCOPY SYSTEM MANUFACTURER. THE INCIDENT INVOLVED A DEVICE (ART. NO.: TM220- 27" FULL HD-MONITOR; SERIAL NO.: (B)(6) MANUFACTURED BY EIZO. BELOW DESCRIPTION OF THE EVENT WERE BASED ON THE INFORMATION PROVIDED BY KARL STORZ SE & CO. KG. THE INCIDENT WITH A LAPAROSCOPY TOWER OCCURRED IN AN INSTITUTION IN COLUMBIA. THE ASSISTING STAFF INDICATES THAT DURING THE SURGICAL PROCEDURE, THE LAPAROSCOPY TOWER WAS TURNED OFF AND WHEN IT WAS TURNED ON, THE IMAGE WAS SHOWN AS A MIRROR IMAGE, CAUSING INJURY TO THE PATIENT. THE PATIENT HAD TO SPEND 15 DAYS IN INTENSIVE CARE. THIS CASE IS ASSOCIATED WITH THE MISUSE OF EQUIPMENT BY THE ASSISTING STAFF, HOWEVER IT COULD NOT BE CLEARLY IDENTIFIED THAT THE MIRROR IMAGE WAS CAUSED BY MISUSE OF THE MONITOR OR MISUSE OF THE ENDOSCOPE SYSTEM. IT WAS ALSO REPORTED THAT KARL STORZ HAD REQUESTED RETURN FOR THE AFFECTED DEVICE FOR FURTHER INVESTIGATION, HOWEVER, THAT THE DEVICE IN QUESTION WON?LT BE RETURNED AS THE KARL STORZ DISTRIBUTOR IN COLUMBIA CONFIRMED MISUSE BY THE CUSTOMER AND THE USED DEVICES ARE IN GOOD CONDITION.
Patient problems: Insufficient Information
MAUDE report 17658127 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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