VanishPoint® 24321Recalls & reported problems
Retractable Technologies, Inc. · 23G x 3/4" w/12" tubing VanishPoint® Blood Collection Set, Without Luer Adapter · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 00613703243201), received between May 23, 2019 and May 23, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Retraction Problem” (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
- Retraction Problem1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 23, 2019Retraction Problem
WHILE USING A VANISHPOINT 23G ON A PATIENT, I CLICKED THE BUTTON AND THE NEEDLE RETRACTED ONLY HALF WAY STOPPED AND THEN 3 SECONDS LATER RETRACTED ALL THE WAY. THIS IS VERY UNSAFE. MANUFACTURER RESPONSE FOR SET, ADMINISTRATION, INTRAVASCULAR, VANISHPOINT (PER SITE REPORTER). MFR SENT CLINICAL REP ALONG WITH TERRITORY MANAGER, WILL BE SENDING TRAINERS NEXT WEEK.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8635471 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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