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VanishPoint® 10301Recalls & reported problems

Retractable Technologies, Inc. · 3mL 25G x 5/8" VanishPoint® Syringe · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00613703103000), received between Mar 20, 2023 and Mar 20, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Component Missing” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Component Missing1

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.

  • MalfunctionMar 20, 2023Component Missing

    NURSE PULLED VANISHPOINT 3ML 25G X 5/8" SYRINGE FROM BOX IN OFFICE PHARMACY. NURSE OBSERVED THE SYRINGE WAS IN A SEALED SLEEVE WITHOUT A CAP OVER THE NEEDLE. NURSE IMMEDIATELY BROUGHT SEALED SYRINGE TO NURSE SUPERVISOR. OTHER SYRINGES IN THE BOX HAD CAPS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16584144 ↗

Other Syringe, Antistick devices

All Syringe, Antistick devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.