FDA Recalls: What Drops Were Affected – Hollywood Life

In April 2026, the U.S. Food and Drug Administration (FDA) issued a recall for a particular brand of cough drops and classified it as a Class II recall. This decision comes as spring often brings a surge in allergies, colds, and coughs, leading many consumers to seek clarity on which specific cough drops have been removed from store shelves. Understanding the details of this recall is crucial for anyone relying on these products for relief during allergy season.

In this article, you will discover the specific cough drops that were voluntarily recalled by their manufacturer, as well as the necessary steps to take if you have already purchased these products. Being informed is essential for your health and safety, especially when it comes to over-the-counter medications.

Which Cough Drops Were Recalled in 2026?

The following Menthol Cough Suppressant products were included in the recall:

• Exchange Select, Menthol Cough Suppressant Oral Anesthetic, Honey Lemon Flavor Cough Drops, 30-count bag; Lot number: 20241030, Exp Date: 10/30/2026, UPC: 614299398870
• Exchange Select, Menthol Cough Suppressant Oral Anesthetic, Cough Drops, Menthol Flavor, 30-count bag; Lot number: 20241030, Exp Date: 10/30/2026, UPC: 614299398887
• Caring Mill, Menthol Cough Suppressant Oral Anesthetic, Cough Drops, Cherry, 90-count bag, distributed by: FSA Store Inc.; Lot number: 20241030, Exp Date: 10/30/2026, UPC: 810025928407
• Discount Drug Mart Food Market, Cough Drops, Menthol Cough Suppressant Anesthetic, Honey Lemon, 30-count bag, distributed by Drug Mart-Food Fair; Lot number: 20241030, Exp Date: 10/30/2026, UPC: 093351037092
• Discount Drug Mart Food Market, Cough Drops, Menthol Cough Suppressant Anesthetic, 30-count bag, distributed by Drug Mart-Food Fair; Lot number: 20241030, Exp Date: 10/30/2026, UPC: 093351037085
• MGC Health, Menthol Cough Suppressant, Oral Anesthetic, Cough Drops, Sugar Free, Honey Lemon, 25-count bag, distributed by Medical Group Care, LLC.; Lot number: 20240524, Exp Date: 05/24/2026; Lot number: 20240720, Exp Date: 07/20/2026; Lot number: 20240730, Exp Date: 07/30/2026, UPC: 383173000085
• MGC Health, Menthol Cough Suppressant, Oral Anesthetic, Cough Drops, Honey Lemon, 30-count bag, distributed by Medical Group Care, LLC.; Lot number: 20240524, Exp Date: 05/24/2026, UPC: 383173000047
• QC Quality Choice, Menthol Cough Suppressant Oral Anesthetic, Cough Drops, Sugar Free, Black Cherry Flavor, 25-count bag, distributed by CDMA, Inc.; Lot number: 20240720, Exp Date: 07/20/2026, UPC: 635515993372
• QC Quality Choice, Menthol Cough Suppressant Oral Anesthetic, Cough Drops, Cherry Flavor, 30-count bag, distributed by CDMA, Inc.; Lot number: 20240524, Exp Date: 05/24/2026; Lot number: 20240720, Exp Date: 07/20/2026, UPC: 635515993372.
• QC Quality Choice, Pectin Oral Demulcent, Throat Soothing Drops, Creamy Strawberry Flavor, 30-count bag, distributed by CDMA, Inc.; Lot number: 20240720, Exp Date: 07/20/2026, UPC: 635515999398
• QC Quality Choice, Menthol Cough Suppressant Oral Anesthetic, Cough Drops, Menthol Flavor, 30-count bag, distributed by CDMA, Inc.; Lot number: 20240720, Exp Date: 07/20/2026; Lot number: 20240524, Exp Date: 05/24/2026, UPC: 635515986718
• QC Quality Choice, Menthol Cough Suppressant Oral Anesthetic, Cough Drops, Vanilla Honey Flavor, 30-count bag, distributed by CDMA, Inc.; Lot number: 20240720, Exp Date: 07/20/2026, UPC: 635515999411

Why Were These Cough Drops Recalled?

The recall of the Menthol Cough Suppressant drops was prompted by findings from a manufacturing facility inspection conducted on August 15, 2025. The FDA recommended this action due to observations that “may bear on product quality,” although they did not disclose specific details regarding the issues discovered. This lack of transparency can concern consumers who rely on these products for relief.

The recall was initiated by Xiamen Kang Zhongyuan Biotechnology Co., Ltd., based in China, on March 20, 2026. Following this, the FDA classified the situation as a Class II recall, which indicates that exposure to a “violative product” could potentially lead to “temporary or medically reversible adverse health consequences,” as outlined by the administration. Understanding the reasons behind this recall can help consumers make informed decisions regarding their health.