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Cough Drops Recall Update: FDA Sets Risk Level

Cough Drops Recall Update: FDA Sets Risk Level

Summary

The FDA has issued a Class II recall for various cough drop products, indicating a moderate risk to users. The recall affects products made by a company in China and sold in the U.S. The affected products should not be used, and consumers are advised to return or dispose of them per distributor instructions.

Key Facts

  • The FDA classified the cough drop recall as Class II, indicating moderate risk.
  • The recall started on March 20, 2026, and is still ongoing with no specified end date.
  • Products were made by Xiamen Kang Zhongyuan Biotechnology Co., Ltd. in China.
  • Affected brand names include Exchange Select, Caring Mill, and others.
  • The cough drops have different flavors like honey lemon and cherry.
  • Expiration dates for the products fall in 2026, with specific lot numbers noted.
  • Products were sold nationwide in the U.S., but no public announcement was made.
  • Consumers are advised to not use the recalled products and consult healthcare providers if adverse symptoms occur.

Source Information