Becton Dickinson & Company recalls PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D
- Recall date
- March 17, 2020
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1946-2020
- FDA classification
- Class II
- Brand / firm
- Becton Dickinson & Company
- Sold / distributed
- AZ, CT, GA, IL, LA, MA, MI, MN, ND, NE, NY, OH, SD, TX),
Why it was recalled
Iincorrectly packaged without the required lidocaine as labeled
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D
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