SOL-M™ Luer Lock Syringe without Needle 180005Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00818392014815), received between Jul 23, 2020 and Jul 23, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Loose or Intermittent Connection” (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 23, 2020Loose or Intermittent Connection

  A DOCTOR (END USER) REPORTED THAT A SOL-M 5ML LUER LOCK SYRINGE W/O NEEDLE LUER LOCK FUNCTION DID NOT WORK CORRECTLY. THEY HAD SCREWED THE CANNULA UNTIL IT CAME DOWN TO THE BOTTOM BUT IT CONTINUED TO SCREW AND IT SHOULD NOT DO SO AS IT SHOULD BE LOCKED. A CANNULA BECAME LOOSE AT HYDRODISSECTION DURING CATARACT SURGERY WHEN IT WAS INSERTED INTO THE EYE CAUSING INTERNAL DAMAGE. PER THE REPORT, PATIENT WAS ADVERSELY AFFECTED BY THE ISSUE, HOWEVER IT IS UNKNOWN IF MEDICAL INTERVENTION WAS REQUIRED. IT IS ALSO UNKNOWN IF SURGERY WAS DELAYED DUE TO THE ISSUE. THE DOCTOR CHECKED AFTER THE EVENT, THEY COULD STILL SPIN CANNULA AND IT WAS NOT LOCKED. THE END USER FACILITY THEN CHECKED ALL 5ML SYRINGES THAT THEY USED AND THEY WERE ALL SIMILAR IN PERFORMANCE (THE LOCK FUNCTION DID NOT WORK CORRECTLY). THE END USER FACILITY COMPARED THEIR OWN SYRINGES AND SOL-M SYRINGES. THEIR SYRINGES COULD NOT BE ROTATED PAST THE BOTTOM POSITION.

  Patient problems: Injury

  MAUDE report 10316064 ↗