Medline Industries, Inc. VAL050CABWCRecalls & reported problems
Medline Industries, Inc. · CATARACT PACK BOSWELL · Class 2
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 10195327029074), received between Aug 22, 2024 and Aug 22, 2024 — classified as 1 injury.
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.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 22, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE CUSTOMER, "THE CUSTOMER REPORTED THEIR MED CUPS HAVE TINY WHITE FIBERS THAT ARE ALL OVER THEM. THIS IS CAUSING ISSUES AS SEVERAL TIMES THESE FIBERS ARE GETTING ON THE INSTRUMENTS AND ENDING UP INSIDE THE PATIENT'S EYE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20042159 ↗
Other Eye tray devices
- Medline Industries, Inc. DYNJ47859CMedline Industries, Inc. · Eye tray5 recalls0 reports
- Medline Industries, Inc. DYNJ68875FMedline Industries, Inc. · Eye tray3 recalls1 report
- Medline Industries, Inc. DYNJ65808CMedline Industries, Inc. · Eye tray3 recalls0 reports
- Medline Industries, Inc. DYNJ902256CMedline Industries, Inc. · Eye tray3 recalls0 reports
- Medline Industries, Inc. DYNJ64572AMedline Industries, Inc. · Eye tray3 recalls0 reports
- Medline Industries, Inc. DYNJ41207CMedline Industries, Inc. · Eye tray3 recalls0 reports
- Medline Industries, Inc. DYNJ53019AMedline Industries, Inc. · Eye tray2 recalls1 report
- Medline Industries, Inc. DYNJ909065AMedline Industries, Inc. · Eye tray2 recalls0 reports
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.
How reports and recalls are matched · Editorial policy · Report an error on this page