Valeritas, Incorporated recalls DEMO No Needle Corrugated Carton 20 U/D, Part Number 2260-03
- Recall date
- July 3, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0195-2020
- FDA classification
- Class II
- Brand / firm
- Valeritas, Incorporated
- Sold / distributed
- Nationwide within U.S.
Why it was recalled
There is a potential for "No Needle Demo Units" to contain a needle.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
DEMO No Needle Corrugated Carton 20 U/D, Part Number 2260-03
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