Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BD Epilor Syringe BD Franklin Lakes Recalled by Becton Dickinson & Company Due to BD has received several reports indicating that the...
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
BD Epilor Syringe BD Franklin Lakes, NJ 07417 BD EDC Laagstraat 57, B-9140 Temse-Belgium The Epilor syringe is used in conjunction with an epidural needle with the purpose of finding the epidural space.
Quantity: 1,335,885 units
Why Was This Recalled?
BD has received several reports indicating that the plunger of the 7 mL BD Epilor plastic BD Luer-Lok Loss of Resistance Syringe may stall or stick within the syringe preventing the user from detecting a loss of resistance upon entering the epidural space.
Where Was This Sold?
This product was distributed to 21 states: AZ, CA, FL, GA, IL, MD, MI, MN, MO, MT, NE, NJ, NY, OH, PA, RI, SC, TN, TX, UT, VA
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