Medicine may not be an exact science, but precision is crucial for patient care. That’s why the presence of unknown particles in injectable vials of Phenylephrine Hydrochloride prompted a recall by ...
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.
The Healthy @Reader's Digest on MSN2d
Another Blood Pressure Medication Has Been Recalled NationwideIt was manufactured by a well-known pharmaceutical company and may be used to treat a specific group of patients managing ...
A blood pressure medication has been recalled from suppliers due to possible “microbial contamination”. Amlodipine is a ...
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 FDA labeled a recall of integrated arterial catheters made by Medline Class I, the most serious kind of recall.
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 ...
Provepharm is recalling lot number 24020027; Expiry Date December 2025 of Phenylephrine hydrochloride Injection, USP, 10 mg/ mL at the hospital/institution ...
The U.S. Food and Drug Administration (FDA) has given its second most serious risk level, Class II, to a product from D. Coluccio & Sons. The recalled product is a 300 gram pack of chocolate chip ...
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