Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-3116-2017 — 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.

U.S. FDA — Device Enforcement · United States · 2017-06-13 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-3116-2017
Date of alert: 2017-06-13
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Becton Dickinson & Company
Product category: device
Product type: Devices

Reported risk: Presence of loose polypropylene foreign matter above release specification.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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