Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

Oxycodone Hydrochloride Oral Solution Recalled by Genus Lifesciences Inc. Due to Presence of Foreign Substance: Particulate matter was found...

Date: December 23, 2020
Company: Genus Lifesciences Inc.
Status: Terminated
Source: FDA (Drug)

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 Genus Lifesciences Inc. directly.

Affected Products

Oxycodone Hydrochloride Oral Solution, USP 5 mg/5mL unit dose cups, Rx Only, Genus Lifesciences Inc. NDC 64950-354-05 Case NDC: 64950-354-450(40 unit dose cups) Case NDC 64950-354-55 (50 unit dose cups)

Quantity: 1,171,550 cups

Why Was This Recalled?

Presence of Foreign Substance: Particulate matter was found in multiple lots of product.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Genus Lifesciences Inc.

Genus Lifesciences Inc. has 1 total recall tracked by RecallDetector.

Related Recalls

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