Class II — Potential Health Hazard

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

Micro-Mate Tuberculin Glass Syringe Recalled by Cadence Inc. Due to Graduation marks of the syringe are not centered...

Date: July 9, 2015
Company: Cadence Inc.
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 Cadence Inc. directly.

Affected Products

Micro-Mate Tuberculin Glass Syringe, Non-sterile Catalog numbers 5208, 5209

Quantity: 1665 units

Why Was This Recalled?

Graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Cadence Inc.

Cadence Inc. has 2 total recalls tracked by RecallDetector.

Related Recalls

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