Class III โ€” Low Risk

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

Oxaydo (oxycodone HCl Recalled by Zyla Life Sciences US Inc. Due to Sub-potent Drug: Lower potency than labeled.

Date: October 20, 2023
Company: Zyla Life Sciences US Inc.
Status: Ongoing
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 Zyla Life Sciences US Inc. directly.

Affected Products

Oxaydo (oxycodone HCl, USP) tablets, 7.5 mg, 100 Tablets per bottle, Rx only, Distributed by: Zyla Life Sciences US Inc., Wayne, PA 19087. NDC: 69344-213-11

Quantity: 3,792 bottles

Why Was This Recalled?

Sub-potent Drug: Lower potency than labeled.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Zyla Life Sciences US Inc.

Zyla Life Sciences US Inc. has 1 total recall tracked by RecallDetector.

Related Recalls

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