FDA recall Z-0207-2018

Product

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.

Distribution

Nationwide Distribution

Key facts

Status

Terminated

Initiation date

2017-05-31

Report date

2017-12-13

Termination date

2018-06-28

Voluntary/Mandated

Voluntary: Firm initiated

Location

Franklin Lakes, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0207-2018