Medline Industries, Inc. LYN030INSPARecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10193489290998), received between Jul 30, 2022 and Jul 30, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJul 30, 2022Device Contamination with Chemical or Other Material

  IT WAS REPORTED THAT THERE IS FABRIC AROUND THE EYE SHIELD, AND EVEN THOUGH EVERYTHING IS PRE-RINSED THE FIBERS STILL SHOW UP. THE FACILITY HAS TO OPEN NEW SYRINGES TO PREVENT FIBERS FROM GETTING IN THE PATIENTS EYES. PARTICULATE WAS IN THE EYE AND REMOVED WITH TYING FORCEPS.

  Patient problems: Foreign Body In Patient

  MAUDE report 15136749 ↗