Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BD Needle 22GA 1-1/2in SafetyGlide(TM) Non Sterile Recalled by Becton Dickinson & Company Due to Presence of loose polypropylene foreign matter above release...
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 Needle 22GA 1-1/2in SafetyGlide(TM) Non Sterile, Bulk, REF 301701 The BD SafetyGlide(TM) needle is intended to be used for general purpose injection, aspiration of fluids from parts of the body below the surface of the skin, injection into intravenous ports and tubings external to the patient. The needle stick prevention feature of the device contains a mechanism that covers the needlepoint after use. Bulk Non Sterile configuration is intended for further manufacturing, processing or repackaging
Quantity: 1,249,200 units
Why Was This Recalled?
Presence of loose polypropylene foreign matter above release specification.
Where Was This Sold?
This product was distributed to 10 states: CA, IL, KS, MI, NY, NC, PA, SC, TX, 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