RecallWatchUSA

Home / Recalls / Medical Devices

Becton Dickinson & Company recalls BD Needle 22GA 1-1/2in SafetyGlide(TM) Non Sterile, Bulk, REF 301701 The BD SafetyGlide(TM) needle is intended to be

Recalled September 20, 2017 · FDA recall Z-3116-2017 · Becton Dickinson &

Hazard
Presence of loose polypropylene foreign matter above release specification. · FDA Class II
Units
1,249,200 units
Sold at
US Distribution to: TX, PA, VA, CA, NY, IL, MI, NC, SC and KS.

Description

Presence of loose polypropylene foreign matter above release specification.

Product
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
Manufacturer(s)
Becton Dickinson & Company

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Becton Dickinson & Company recalls BD Needle 22GA 1-1/2in SafetyGlide(TM) Non Sterile, Bulk, REF 301701 The BD SafetyGlide(TM) needle is intended to be | RecallWatchUSA