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Cough Drops Sold Nationwide Recalled: FDA

The FDA classified the recalled cough drops as Class II, meaning use could cause temporary or medically reversible health consequences.

  • On Monday, the Food and Drug Administration announced a nationwide voluntary recall of various private-label cough drops and throat lozenges. Chinese manufacturer Xiamen Kang Zhongyuan Biotechnology initiated the action, affecting products sold across multiple U.S. retailers.
  • Following an August 15, 2025, FDA inspection of the facility, officials noted 'certain observations' that potentially impact product quality, prompting the company to initiate the voluntary recall last month.
  • Products sold under Exchange Select, Caring Mill, Discount Drug Mart Food Market, MGC Health, and QC Quality Choice are impacted. The FDA issued a Class II recall, meaning exposure may cause 'temporary or medically reversible adverse health consequences.'
  • The FDA has not disclosed the total number of units included in this nationwide recall, though the agency considers serious health effects from the products to be remote.
  • Watchdog Teresa Murray of the U.S. Public Interest Research Group recommends checking recall lists weekly to ensure consumer safety, as regulators and companies often negotiate fixes for months or years.
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Cough drops sold nationwide recalled: FDA

A China-based company is voluntarily recalling numerous cough drop products sold across the U.S., according to the Food and Drug Administration.

·Washington, United States
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PIX 11 broke the news in New York, United States on Monday, April 13, 2026.
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