Medicine may not be an exact science, but precision is crucial for patient care. That’s why the presence of unknown particles ...
An injectable blood pressure drug has been recalled after the FDA has warned it could cause side effects, such as stroke or death.
It was manufactured by a well-known pharmaceutical company and may be used to treat a specific group of patients managing hypertension.
It's not the only blood pressure medication recall to happen in recent months, but the FDA's concern appears to follow a common theme.
A Pennsylvania-based pharmaceutical firm and the FDA issued a recall of an injectable blood pressure medicine after a customer noticed "a visible black particulate matter" in a vial. Dr. Bernard Ashby ...
A blood pressure medication has been recalled from suppliers due to possible “microbial contamination”. Amlodipine is a ...
The FDA labeled a recall of integrated arterial catheters made by Medline Class I, the most serious kind of recall.
The FDA says administering a drug containing particulate matter may cause local irritation or swelling. If the particulates enter blood vessels, it can travel to various organs and potentially ...
The recall affects one lot of phenylephrine hydrochloride injection, 10mg/ml, sold to wholesalers, distributors, compounding companies and hospitals. The drug is used to treat low blood pressure ...