News

Infectious disease doctors at University Hospitals Cleveland Medical Center linked a woman's blindness to EzriCare Artificial Tears before the FDA recall.

Akorn Operating Company issued a voluntary recall of all of its products because it can no longer guarantee their safety.

The FDA has received 346 death reports and more than 98,000 medical device reports linked to recalled Philips CPAP machines since April 2021.

The FDA and CDC warned consumers to stop using EzriCare Artificial Tears and Delsam Pharma’s Artificial Tears in light of reports of serious health risks.

The U.S. Preventative Screening Task Force recently came out against routine OSA screenings, citing insufficient evidence of benefits.

The judgment upheld an earlier dismissal by a lower-level federal court in Florida, finding that the Zantac lawsuit was improperly framed.

The problem stems from supply chain issues and an increased number of people being prescribed the drug, a stimulant used mainly to treat ADHD.