Becton Dickinson & Company recalls BD MicrotainerTubes with K2E (K2EDTA) Catalog Number: 365974
- Recall date
- May 13, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0057-2020
- FDA classification
- Class II
- Brand / firm
- Becton Dickinson & Company
- Sold / distributed
- Nationwide Foreign: AR AU BE BN BR CA CL CN CO CR CW EC GT GY HK HN ID IN JP KR MX MY NI NZ PA PE PG PH PK SG SR SV TH TW UY VN
Why it was recalled
Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
BD MicrotainerTubes with K2E (K2EDTA) Catalog Number: 365974
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