Class III โ€” Low Risk

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

Cyproheptadine Hydrochloride Syrup Recalled by Lyne Laboratories, Inc. Due to Subpotency: product assayed and found OOS for cyproheptadine

Date: June 7, 2016
Company: Lyne Laboratories, 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 Lyne Laboratories, Inc. directly.

Affected Products

Cyproheptadine Hydrochloride Syrup, Oral Solution USP, 2 mg/5 mL, packaged in an amber glass 473 mL (one pint) bottle with child-resistant screw closure, Rx only, Distributed by: Rising Pharmaceuticals, Inc., Allendale, NJ 07401, Manufactured by: Lyne Laboratories, Inc., Brockton, MA 02301, NDC 64980-0504-48

Quantity: 12,215 Bottles shipped to Rising Pharmaceuticals

Why Was This Recalled?

Subpotency: product assayed and found OOS for cyproheptadine

Where Was This Sold?

This product was distributed to 1 state: NJ

Affected (1 state)Not affected

About Lyne Laboratories, Inc.

Lyne Laboratories, Inc. has 4 total recalls tracked by RecallDetector.

Related Recalls

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