Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

BNX Fine Need Aspiration System (22GA) Recalled by Medtronic Due to Handle may break during use.

Date: February 8, 2017
Company: Medtronic
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Medtronic directly.

Affected Products

BNX Fine Need Aspiration System (22GA); Material/Part#: DSN-22-01

Quantity: 1,096 Units (total for all products)

Why Was This Recalled?

Handle may break during use.

Where Was This Sold?

This product was distributed to 40 states: AL, AZ, AR, CA, CO, CT, DE, FL, GA, HI, IL, IN, IA, KS, LA, MD, MA, MI, MN, MO, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SC, SD, TN, TX, VA, WA, WI, DC

Affected (40 states)Not affected

About Medtronic

Medtronic has 47 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report