Class III — Low Risk

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

Midol Complete Recalled by Bayer Healthcare, LLC Due to Labeling: Label Mix-up: This recall was initiated after...

Date: April 26, 2012
Company: Bayer Healthcare, LLC
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 Bayer Healthcare, LLC directly.

Affected Products

Midol Complete, Acetaminophen, Caffeine, Pyrilamine Maleate, Gelcaps 24 ct. blister, OTC, Distributed by Bayer Health Care, Morristown, NJ 07962 NDC 0280-8015-24

Quantity: 119,412 cartons

Why Was This Recalled?

Labeling: Label Mix-up: This recall was initiated after identifying that the label statement on the blister strip regarding the maximum number of capsules/caplets that should be taken within a 24-hour period, does not match the statement on the carton.

Where Was This Sold?

Product was distributed to 93 retail accounts/customers.

About Bayer Healthcare, LLC

Bayer Healthcare, LLC has 4 total recalls tracked by RecallDetector.

Related Recalls

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