Phadia US Inc recalls Phadia 1000 Instrument, Article Number 12-3800-01.
- Recall date
- July 5, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0387-2018
- FDA classification
- Class II
- Brand / firm
- Phadia US Inc
- Sold / distributed
- Nationwide
Why it was recalled
The "Retry" command does not function properly which could cause a shortage of Wash and Rinse solution and affect assay performance and test 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
Phadia 1000 Instrument, Article Number 12-3800-01.
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