Class II — Potential Health Hazard

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

RX-2 COUDE Epidural Needle Recalled by Epimed International Due to Potential for partially incomplete seal of product, impacting...

Date: July 24, 2017
Company: Epimed International
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 Epimed International directly.

Affected Products

RX-2 COUDE Epidural Needle, 16g x 3.5in (8.9cm)TW, 10 units, Calibrated, Plastic Hub, Detachable Wing, Blunt Stylet, Sterile, Rx only, For Use with 19g or Smaller Catheter

Quantity: 500 units

Why Was This Recalled?

Potential for partially incomplete seal of product, impacting sterility.

Where Was This Sold?

This product was distributed to 13 states: AR, CA, IN, IA, KY, LA, MI, NY, OH, OR, TN, TX, WA

Affected (13 states)Not affected

About Epimed International

Epimed International has 7 total recalls tracked by RecallDetector.

Related Recalls

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