Class III โ€” Low Risk

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

PE Daytime Cold/Flu LiqGel Recalled by L. Perrigo Co. Due to Subpotent; 12 month time point for the active...

Date: February 18, 2013
Company: L. Perrigo Co.
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 L. Perrigo Co. directly.

Affected Products

PE Daytime Cold/Flu LiqGel, Multi Symptom Relief, Acetaminophen/Dextromethorphan HBr/Phenylephrine HCL 325/10/5 mg gel caps 20 count blister pack, Distributed By: Wal-Mat Stores Inc., Bentonville, AR, 72716

Quantity: 60,048 Blister packs

Why Was This Recalled?

Subpotent; 12 month time point for the active ingredient Phenylephrine HCl.

Where Was This Sold?

This product was distributed to 1 state: AR

Affected (1 state)Not affected

About L. Perrigo Co.

L. Perrigo Co. has 7 total recalls tracked by RecallDetector.

Related Recalls

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