Showing 1 to 7 of 7 results
FDA Warns Against Walmart Shrimp Due to Radioactive Contamination
The FDA issued a "Do Not Eat" warning for Walmart's Great Value raw frozen shrimp due to Cesium-137 contamination discovered in shipments from Indonesia to four major US ports; all contaminated shipments were blocked from entering the US.
FDA Warns Against Walmart Shrimp Due to Radioactive Contamination
The FDA issued a "Do Not Eat" warning for Walmart's Great Value raw frozen shrimp due to Cesium-137 contamination discovered in shipments from Indonesia to four major US ports; all contaminated shipments were blocked from entering the US.
Progress
56% Bias Score
FDA Issues Safety Warnings for Boston Scientific Heart Devices
The FDA issued safety warnings for two Boston Scientific heart devices—the Endotak Reliance defibrillator, linked to 386 serious injuries and 16 deaths, and the Watchman device, linked to 120 serious injuries and 17 deaths—prompting concerns about device safety and the company's financial standing.
FDA Issues Safety Warnings for Boston Scientific Heart Devices
The FDA issued safety warnings for two Boston Scientific heart devices—the Endotak Reliance defibrillator, linked to 386 serious injuries and 16 deaths, and the Watchman device, linked to 120 serious injuries and 17 deaths—prompting concerns about device safety and the company's financial standing.
Progress
24% Bias Score
FDA Warns of Diabetes App Notification Failures Leading to Deaths
The FDA warned that missed smartphone notifications from diabetes management apps have led to dangerously low blood sugar and death, affecting 37 million Americans with diabetes; they recommend regular checks of phone settings to ensure alerts function correctly.
FDA Warns of Diabetes App Notification Failures Leading to Deaths
The FDA warned that missed smartphone notifications from diabetes management apps have led to dangerously low blood sugar and death, affecting 37 million Americans with diabetes; they recommend regular checks of phone settings to ensure alerts function correctly.
Progress
48% Bias Score
FDA Issues Black Box Warning for Menopausal Hot Flash Drug Veozah
The FDA issued a black-box warning for Veozah, a non-hormonal drug treating menopausal hot flashes, due to rare but serious liver injury risk, mandating increased blood tests and immediate treatment cessation upon symptom onset; nearly 29,000 patients used it in May 2024.
FDA Issues Black Box Warning for Menopausal Hot Flash Drug Veozah
The FDA issued a black-box warning for Veozah, a non-hormonal drug treating menopausal hot flashes, due to rare but serious liver injury risk, mandating increased blood tests and immediate treatment cessation upon symptom onset; nearly 29,000 patients used it in May 2024.
Progress
32% Bias Score
FDA Warns Against Unapproved Mousse Sunscreens
The FDA warned five companies, including Supergoop! and Vacation Inc., about their mousse sunscreens lacking approval and posing ingestion risks due to food-like packaging.
FDA Warns Against Unapproved Mousse Sunscreens
The FDA warned five companies, including Supergoop! and Vacation Inc., about their mousse sunscreens lacking approval and posing ingestion risks due to food-like packaging.
Progress
40% Bias Score
FDA Warns of Serious Side Effects from Online Topical Finasteride
The FDA warned about serious side effects, including sexual dysfunction and suicidal ideation, from unapproved topical finasteride hair-loss treatments sold online by telehealth companies like Hims, Hers, and Ro, with 32 complaints filed between 2019 and 2024.
FDA Warns of Serious Side Effects from Online Topical Finasteride
The FDA warned about serious side effects, including sexual dysfunction and suicidal ideation, from unapproved topical finasteride hair-loss treatments sold online by telehealth companies like Hims, Hers, and Ro, with 32 complaints filed between 2019 and 2024.
Progress
64% Bias Score
FDA Issues Black Box Warning for Veozah Due to Liver Damage Risk
The FDA issued a black box warning for the drug Veozah, used to treat hot flashes, due to rare but serious liver damage, mandating frequent blood tests and immediate reporting of symptoms.
FDA Issues Black Box Warning for Veozah Due to Liver Damage Risk
The FDA issued a black box warning for the drug Veozah, used to treat hot flashes, due to rare but serious liver damage, mandating frequent blood tests and immediate reporting of symptoms.
Progress
32% Bias Score
Showing 1 to 7 of 7 results