Becton Dickinson & Company recalls BD Precision Glide Needle 18G x 1 RB, Catalog 305195 Product Usage: These needles are intended for general purpose flui…
- Recall date
- May 31, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0207-2018
- FDA classification
- Class II
- Brand / firm
- Becton Dickinson & Company
- Sold / distributed
- Nationwide Distribution
Why it was recalled
Hub damage resulting in breakage and/or leakage during use.
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 Precision Glide Needle 18G x 1 RB, Catalog 305195 Product Usage: These needles are intended for general purpose fluid injection/aspiration, infusion, venipuncture to obtain blood collection and insulin injection.
Get recall alerts
Free email alert whenever Becton Dickinson & Company has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Becton Dickinson & Company