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Terminated

BD 5ml Syringe Luer-Lok" Tip with Blunt Fill Needle 18G x 1 1/2 (1.2mm x 40mm) Catalog #305062

FDA Recall Z-2747-2017 · Posted None

Recalling FirmBecton Dickinson & Company
Recall StatusTerminated
Product CodeFMF
Date Initiated2016-09-16
Date Terminated2018-03-20
Product Quantity22,400 units

Reason for Recall

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

Firm Action

BD sent recall letter/return response form on 9/16/2016.

Root Cause

Process control

Distribution Pattern

Nationwide Distribution

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K110771BD SINGLE USE, HYPODERMIC SYRINGEBecton, Dickinson and Company · 2011-05-13

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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