Veeda VDTSP16USRecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00810462020023), received between Dec 9, 2022 and Dec 13, 2022 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Failure to Align” (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 16, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 13, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  A GOVERNMENT AGENCY REPORTED THAT AN OPHTHALMIC OPERATING CONSOLE PRESENTED PROBLEMS WITH INTERNAL ILLUMINATOR BURNT OUT DURING A SURGERY. THE PROCEDURE DETAILS AND PATIENT IMPACT HAVE NOT BEEN PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15968919 ↗
• MalfunctionDec 12, 2022Inability to Irrigate; Inability to Irrigate

  AN OPHTHALMIC SURGEON REPORTED IRRIGATION COULD NOT BE PERFORMED AND IT DID NOT COME OUT AT ALL DURING A SURGERY. THE SURGERY TYPE WAS UNKNOWN. THE SURGERY WAS COMPLETED AFTER REPLACING THE PRODUCT WITH ANOTHER ONE. THERE WAS NO PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15958944 ↗
• MalfunctionDec 9, 2022Failure to Align; Failure to Align

  A HEALTHCARE PROFESSIONAL REPORTED A PATIENT WITH FLAP WAS NOT CUT CORRECTLY INTO THE CORNEA, BUT MAINLY INTO THE PATIENT INTERFACE. PATIENT IMPACT WAS UNKNOWN INITIALLY. THERE ARE MULTIPLE RELATED REPORTS FOR THIS FACILITY. THIS REPORT ADDRESSES A PATIENT INTERFACE (PI) ((B)(4)) AND ADDITIONAL MANUFACTURER REPORTS WILL BE FILED. THERE ARE MULTIPLE RELATED REPORTS FOR THIS EVENT. THIS REPORT ADDRESSES THE UNKNOWN PATIENT'S LEFT EYE AND OTHER MANUFACTURER REPORTS WILL BE FILED.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 15950389 ↗
• MalfunctionDec 9, 2022Fluid/Blood Leak; Fluid/Blood Leak

  A PHYSICIAN LEAKAGE OF BALANCED SALT SOLUTION (BSS) OCCURRED DURING A CATARACT SURGERY. THE SURGERY WAS COMPLETED AFTER REPLACING THE PRODUCT WITH ANOTHER ONE. THERE WAS NO PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15948790 ↗