RecallRadar

FDA Device recall Z-2748-2017

BD SafetyGlide" Injection Needle Catalog #305917 The SafetyGlide " needle is intended to be used for general purpose injection, aspiration…

On 2017-07-26 the FDA classified a Class II recall of BD SafetyGlide" Injection Needle Catalog #305917 The SafetyGlide " needle is intended to be used for general purpose injection, aspiration… by Becton Dickinson And, citing BD identified that several lots did not receive the specified dose of irradiation necessary to meet the Sterility Assurance Level (SAL) required.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2748-2017
ClassificationClass II
Statusterminated
Initiated2016-09-16
Published2017-07-26
Last updated2026-09-13 11:54 UTC
CompanyBecton Dickinson And
DistributionUS

Product

BD SafetyGlide" Injection Needle Catalog #305917 The SafetyGlide " 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 needlestick prevention feature of the device contains a mechanism that covers the needlepoint after use. In the activated position the needle cover guards against accidental needle sticks during normal handling and disposal of the used needle/syringe combination

Reason

BD identified that several lots did not receive the specified dose of irradiation necessary to meet the Sterility Assurance Level (SAL) required.

Identifiers

code_info6022838 2021-01

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2748-2017%22

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