FDA Warns Of Missed Alerts On Phone-Connected Diabetes Devices, Leading To 'Serious Harm'
The FDA issued an alert warning diabetes patients and caregivers about potential issues with smartphone alerts for continuous glucose monitors.
A drug got recalled after someone saw ‘black matter’ that can cause stroke or death
“If the particulate matter enters the blood vessels, it can travel to various organs and potentially block blood vessels in ...
Nationwide Blood Pressure Drug Recall As FDA Issues Fatal Warning
An injectable blood pressure drug has been recalled after the FDA has warned it could cause side effects, such as stroke or death.
ConsumerAffairs4d
Alvogen recalls Fentanyl Transdermal System 25 patches
Alvogen has issued a nationwide recall of one lot of Fentanyl Transdermal System 25 patches because the patches may stick ...
Morningstar9d
Alvogen Issues Voluntary Nationwide Recall for One Lot of Fentanyl Transdermal System 25 mcg/h Due to a Defective Delivery System
MORRISTOWN, N.J., Jan. 31, 2025 /PRNewswire/ -- Alvogen, Inc. is voluntarily recalling one lot of Fentanyl Transdermal System 25 mcg/h transdermal patches to the consumer level. The reason for ...
Tonix Pharmaceuticals Recently Announced Preliminary Full Year 2024 Operating Results and Year-End Cash
Company had $98.8 million in cash as of December 31, 2024; existing cash expected to fund planned operations into the first quarter of ...
Miami Herald14d
A drug got recalled after someone saw ‘black matter’ that can cause stroke or death
Then, tell the FDA’s MedWatch Adverse Event Reporting Program, either online or by calling 800-332-1088 to request a reporting form. Since 1989, David J. Neal’s domain at the Miami Herald has ...
ConsumerAffairs13d
Drug used to treat low blood pressure recalled
Provepharm is recalling lot number 24020027; Expiry Date December 2025 of Phenylephrine hydrochloride Injection, USP, 10 mg/ ...