PlainRecalls
FDA Devices Moderate Class II Terminated

BD Precision Glide Needle 18G x 1 RB, Catalog 305195 Product Usage: These needles are intended for general purpose fluid injection/aspiration, infusion, venipuncture to obtain blood collection and insulin injection.

Reported: December 13, 2017 Initiated: May 31, 2017 #Z-0207-2018

Product Description

BD Precision Glide Needle 18G x 1 RB, Catalog 305195 Product Usage: These needles are intended for general purpose fluid injection/aspiration, infusion, venipuncture to obtain blood collection and insulin injection.

Reason for Recall

Hub damage resulting in breakage and/or leakage during use.

Details

Units Affected
2,598,000 units
Distribution
Nationwide Distribution
Location
Franklin Lakes, NJ

Frequently Asked Questions

What product was recalled?
BD Precision Glide Needle 18G x 1 RB, Catalog 305195 Product Usage: These needles are intended for general purpose fluid injection/aspiration, infusion, venipuncture to obtain blood collection and insulin injection.. Recalled by Becton Dickinson & Company. Units affected: 2,598,000 units.
Why was this product recalled?
Hub damage resulting in breakage and/or leakage during use.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 13, 2017. Severity: Moderate. Recall number: Z-0207-2018.