Vacuette 450040Recalls & reported problems
Greiner Bio-One GmbH · VACUETTE® VISIO PLUS Needle 21G x 1 1/2" green, sterile, not made with natural rubber latex 0.8 x 38 mm · Class 2
Data updated Oct 16, 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 29120017570053), received between Feb 21, 2020 and Feb 21, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Disconnection” (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 16, 2026.
Most reported problems
Device problems
- Disconnection1
Patient problems
- Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 21, 2020Disconnection
CUSTOMER STATES NEEDLE HAS DISCONNECTED FROM THE HOLDER BEFORE AND DURING PHLEBOTOMY; TODAY'S INCIDENT RESULTED IN A PATIENT INJURY. CUSTOMER CONFIRMS NEEDLE DOES NOT BREAK, BUT DISCONNECTS. CUSTOMER STATES "NO" TO ALL EXPOSURE/INJURY QUESTIONS. TRAINING WAS PERFORMED BY SALES REP.
Patient problems: Injury
MAUDE report 9739881 ↗
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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 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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