FDA Recalls Blood Pressure Drug Over ‘Visible Black’ Contaminants
Medicine may not be an exact science, but precision is crucial for patient care. That’s why the presence of unknown particles ...
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FDA recalls blood pressure drug after potentially fatal contamination | Morning in America
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 ...
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.
MLive12d
Blood pressure drug used nationwide recalled by FDA over foreign material that can be fatal
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 ...
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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/ ...
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Another Blood Pressure Medication Has Been Recalled Nationwide
It was manufactured by a well-known pharmaceutical company and may be used to treat a specific group of patients managing hypertension.
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Nearly 1,000 Bottles of a Blood Pressure Medication Recalled Nationwide
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.
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Medline has a Class I arterial catheter recall
The FDA labeled a recall of integrated arterial catheters made by Medline Class I, the most serious kind of recall.
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 the heart, lungs or brain, leading to serious complications such as stroke ...
Cookies Recall Update as FDA Sets Risk Level
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 ...