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Medline Industries, Inc. VAL002CATSDRecalls & reported problems

Medline Industries, Inc. · THE SURGERY CENTER CATARACT · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
3
Deaths reported
0
Injuries reported
3
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10193489259063), received between Dec 7, 2020 and Dec 7, 2020 — classified as 3 injuries.

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

  • Adverse Event Without Identified Device or Use Problem3

Patient problems

  • Unspecified Infection3

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • InjuryDec 7, 2020Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT A PATIENT EXPERIENCED AN UNSPECIFIED INFECTION.

    Patient problems: Unspecified Infection

    MAUDE report 10963417 ↗
  • InjuryDec 7, 2020Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT A PATIENT EXPERIENCED AN UNSPECIFIED INFECTION.

    Patient problems: Unspecified Infection

    MAUDE report 10963375 ↗
  • InjuryDec 7, 2020Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT A PATIENT EXPERIENCED AN UNSPECIFIED INFECTION.

    Patient problems: Unspecified Infection

    MAUDE report 10963307 ↗

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Sources and updates

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