Class II — Potential Health Hazard

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

Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due to Manufacturing defect was found for the cartridge component,...

Date: April 30, 2019
Company: Cardinal Health 200, LLC
Status: Completed
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 Cardinal Health 200, LLC directly.

Affected Products

Monoject Standard Hypodermic Needle, 14 G x 1-1/2" Item code: 8881200011

Quantity: N/A

Why Was This Recalled?

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Cardinal Health 200, LLC

Cardinal Health 200, LLC has 275 total recalls tracked by RecallDetector.

Related Recalls

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