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The consumer healthcare company is recalling the cough syrup, sold under the brand name "Robitussin Honey CF Max Day Adult" in 4-ounce and 8-ounce doses, along with its 8-ounce night-time version.
Robitussin Honey CF Max Nighttime Adult, 8 oz.: Lot T08742, expiration date June 30, 2026 (will read on the packaging as "30JUN2026") Related: What the FDA Ruling on Decongestants Means for You
Robitussin Honey CF Max NT Adult 8oz Lots: T08740 (June 30, 2026), T08742 (June 30, 2026) The elderly and very young people are most likely to experience complications from fungemia.
Haleon is recalling eight lots of Robitussin cough syrup sold nationwide due to a microbial contamination. Consumers with questions can contact Haleon by phone at 1-800-245-1040 or by email at ...
A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall. [1]
2021 – Butterball recalled over 14,000 lbs of turkey meat due to suspected plastic contamination. [109] [110] 2022 – Abbott Nutrition recalled Similac baby formula after the death of an infant from Cronobacter sakazakii. [111] The recall caused significant shortages in baby formula across the United States. [112]
Acute toxicity describes the adverse effects of a substance that result either from a single exposure [1] or from multiple exposures in a short period of time (usually less than 24 hours). [2] To be described as acute toxicity, the adverse effects should occur within 14 days of the administration of the substance. [2]
Robitussin cough syrup is being recalled due to microbial contamination that can lead to fungemia. Honey flavors are included in the 2024 recall.