Bayer recalls one lot of Alka-Seltzer product
This article was originally published in The Tan Sheet
Executive Summary
Bayer Consumer Care recalls lot 296939L of Alka-Seltzer Plus Day & Night Cold Formula liquid gels because the labeling on the foil blister cards in some packages was reversed. The Morristown, N.J., firm said Dec. 8 that less than 4 percent of the lot placed the label for the green night product on the blue day product and vice versa. The company acknowledged consumers may be at risk if they are unaware that an antihistamine in the product could make them drowsy
You may also be interested in...
Keeping Track: Submissions Galore Start The New Year; US FDA Clears New Indications For Enhertu, Xalkori
The latest drug development news and highlights from the Pink Sheet US FDA Performance Tracker
Vaccination Health Next Stop For Dentovations’ Self+ Immunity Supplement Line
Vacci Prep is first “supplement to establish a standard of care for consumers when preparing their immune system for vaccinations,” Dentovations says.
Balancing Innovation And Safety – The US and Australian Medtech Regulatory Systems Compared
Effective medical device regulation supports both safety and innovation needs. This article assesses how well the US FDA and the Australian TGA achieve this balance.
Need a specific report? 1000+ reports available
Buy Reports
Register for our free email digests: