Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge Recalled by Becton Dickinson & Company Due to Iincorrectly packaged without the required lidocaine as labeled
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Becton Dickinson & Company directly.
Affected Products
PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D
Quantity: 655 kits
Why Was This Recalled?
Iincorrectly packaged without the required lidocaine as labeled
Where Was This Sold?
This product was distributed to 14 states: AZ, CT, GA, IL, LA, MA, MI, MN, NE, NY, ND, OH, SD, TX
About Becton Dickinson & Company
Becton Dickinson & Company has 169 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report