Medtronic recalls BNX Fine Need Aspiration System (19GA); Material/Part #: DSN-19-01

Recall date

February 8, 2017

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1472-2017

FDA classification

Class II

Brand / firm

Medtronic

Sold / distributed

US Distribution to AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, VA, WA, WI; and countries of DK and DE

Why it was recalled

Handle may break during use.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

BNX Fine Need Aspiration System (19GA); Material/Part #: DSN-19-01