Class II — Potential Health Hazard

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

Phadia 1000 Instrument Recalled by Phadia US Inc Due to The "Retry" command does not function properly which...

Date: July 5, 2017
Company: Phadia US 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 Phadia US Inc directly.

Affected Products

Phadia 1000 Instrument, Article Number 12-3800-01.

Quantity: 70 units

Why Was This Recalled?

The "Retry" command does not function properly which could cause a shortage of Wash and Rinse solution and affect assay performance and test results.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Phadia US Inc

Phadia US Inc has 9 total recalls tracked by RecallDetector.

Related Recalls

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