Drug Recall: Robitussin Honey CF Adult Cough Syrups

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US/Silver Spring: Haleon US Inc., a Warren, New Jersey establishment and a subsidiary of Haleon Group of Companies of Weybridge, England recalls certain batch/lots of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult Cough Syrups from the American marketplace due to suspected unspecified bacterial contamination and consequential risks of bacterial infection, severe illness and/or possible life-changing complications, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

FDA: https://buff.ly/493NBlB

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/haleon-issues-voluntary-nationwide-recall-robitussin-honey-cf-max-day-adult-and-robitussin-honey-cf

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Cough Syrups are subject to this recall: