Company Recalls Children’s Robitussin and Dimetapp Cough Medicine

  • 📰 thebump
  • ⏱ Reading Time:
  • 74 sec. here
  • 3 min. at publisher
  • 📊 Quality Score:
  • News: 33%
  • Publisher: 51%

Business News News

Business Business Latest News,Business Business Headlines

FDA Announces Recall for Children’s Robitussin and Dimetapp Cough Medicine

On Thursday, June 18 GlaxoSmithKline Consumer Healthcare, a pharmaceutical company, recalled two products: two lots of Children’s Robitussin Honey Cough and Chest Congestion and one lot of Children’s Dimetapp Cold and Cough., the products included incorrect dosing cups in their packaging. The dosing cups for the Children’s Robitussin Honey product are missing the 5mL and 10mL graduations, while the dosing cups for the Children’s Dimetapp are missing the 10mL graduation.

“There is a potential risk of accidental overdose if caregivers dispensing the syrup do not notice the discrepancies between the graduations printed on the dosing cups and the indicated amounts to be administered ,” the FDA wrote in theThe lots were distributed nationwide between February 5, 2020 and June 3, 2020. The lots affected by the recall are:

**Children’s Robitussin Honey Cough and Chest Congestion DM **NDC 0031-8760-12 Lots: 02177 and 02178 According to the FDA, symptoms of overdose of either product may include brain stimulation causing increase in energy, elevation in blood pressure, heart rate, and respiration; severe dizziness or drowsiness; fainting; seizure; decreased respiration; nausea; vomiting; constipation; diarrhea; abdominal pain; urinary retention and more.

The announcement states, “As of the date of the recall announcement, GSK Consumer Healthcare has not received any adverse events related to these products or consumer complaints regarding the incorrect dosing cups supplied with the product.” GSK Consumer Healthcare has also notified wholesalers, distributors and retailers to arrange to return any recalled products. Those who have existing inventory of the recalled lots should stop distribution and quarantine these lots immediately.

For consumers who have questions about the recall or would like to report an adverse reaction, call 1-800-762-4675 Monday through Friday from 8 a.m. to 6 p.m. EST.

 

Thank you for your comment. Your comment will be published after being reviewed.
Please try again later.
We have summarized this news so that you can read it quickly. If you are interested in the news, you can read the full text here. Read more:

 /  🏆 702. in BUSİNESS

Business Business Latest News, Business Business Headlines