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 ...

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.

An injectable blood pressure drug has been recalled after the FDA has warned it could cause side effects, such as stroke or death.

The specifically recalled chips were: 13-ounce bags of Lay's Classic Potato Chips with UPC of 28400 31041, a "Guaranteed ...

A blood pressure medication has been recalled from suppliers due to possible “microbial contamination”. Amlodipine is a ...

Medicine may not be an exact science, but precision is crucial for patient care. That’s why the presence of unknown particles ...

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 ...

Phenylephrine hydrochloride injection is commonly used in patients undergoing anesthesia. Provepharm has said no adverse events have been linked to the recall. Healthcare providers and distributors ...

Pennsylvania-based pharmaceutical firm Provepharm Inc is voluntarily recalling vials of phenylephrine hydrochloride, which is ...

Provepharm is recalling lot number 24020027; Expiry Date December 2025 of Phenylephrine hydrochloride Injection, USP, 10 mg/ ...