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Vacuette 456003Recalls & reported problems

Greiner Bio-One GmbH · VACUETTE® TUBE 6 ml K3E K3EDTA 13x100 pink cap-black ring, non-ridged, USA · Class 2

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier.

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.

Recalls naming this device

  1. Mar 31, 2023Completed

    Some of the tubes may be incorrectly labeled.

    Z-1583-2023 · Root cause: Labeling Change Control · Recall details · FDA record ↗

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Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page