Class II — Potential Health Hazard

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

EZ-IO 45mm (40kg & up) Needle Set Recalled by Vidacare Corporation Due to The voluntary recall is due to the needle...

Date: March 31, 2014
Company: Vidacare Corporation
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 Vidacare Corporation directly.

Affected Products

EZ-IO 45mm (40kg & up) Needle Set, part number 9079-VC-005; lot code 3606455

Quantity: 172

Why Was This Recalled?

The voluntary recall is due to the needle set not meeting its specifications.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Vidacare Corporation

Vidacare Corporation has 2 total recalls tracked by RecallDetector.

Related Recalls

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