Multiple Brands of Eye Drops Recalled Due to Infection Risks
The recalled eye drops have been linked to reports involving a variety of complaints, including burning eyes, distorted vision, and vision loss.
The recalled eye drops have been linked to reports involving a variety of complaints, including burning eyes, distorted vision, and vision loss.
The FDA warns that the recalled syringes could cause infections, blood loss, increased blood clot risks, embolism and death.
Lack of timely testing and adequate syphilis treatment during pregnancy contributed to nearly 90% of all congenital syphilis cases reported in 2022, according to the CDC.
Researchers warn that older patients kept overnight in the ER face higher risks of heart attacks, strokes, infections and other adverse health events.
The FDA advises consumers to avoid the potentially dangerous eye drops, which may still be available for consumers to purchase and use in some locations
In some cases, nursing home patients on ventilators were several times more likely to develop treatment-resistant infections than those on ventilators in hospitals.
Eight companies have received FDA warning letters over the sale of illegal and unapproved eye products, including eye drops marketed for conditions that were never approved, and some that contain dangerous ingredients.
FDA sampling and testing has confirmed bacterial and fungal contamination in at least one lot of Dr. Berne’s recalled eye drops, which have been linked to adverse event reports
One out of every three hospital deaths involves a sepsis diagnosis, according to CDC officials, which issued new guidelines to reduce the risk of hospital infections.
FDA sampling and testing found bacterial and fungal contamination in Dr. Berne's and LightEyez eye drops which could carry risks of vision loss and death.