Class III โ€” Low Risk

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

Aptensio XR (methylphenidate HCl extended-release) capsules 15 mg Rx Only Recalled by Rhodes Pharmaceuticals, L.P. Due to Failed Dissolution Specification: Low dissolution outside of specifications

Date: April 17, 2018
Company: Rhodes Pharmaceuticals, L.P.
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 Rhodes Pharmaceuticals, L.P. directly.

Affected Products

Aptensio XR (methylphenidate HCl extended-release) capsules 15 mg Rx Only 90-count bottle. Marketed by: Rhodes Pharmaceuticals L.P., Coventry, RI 02816. Manufactured by: Patheon Manufacturing Services LLC, Greenville, NC 27834. NDC 42858-402-45

Quantity: 2454 bottles

Why Was This Recalled?

Failed Dissolution Specification: Low dissolution outside of specifications

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Rhodes Pharmaceuticals, L.P.

Rhodes Pharmaceuticals, L.P. has 2 total recalls tracked by RecallDetector.

Related Recalls

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