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Scammers Make Millions Selling Nonexistent Ozempic, Report Finds

McAfee researchers uncovered 176,871 phishing emails attempting to bait consumers for weight-loss drugs.

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Hologic, Inc Recalls BioZorb Marker Due to Complications with Implanted Devices

The U.S. Food and Drug Administration (FDA) has issued a recall of the Hologic, Inc. BioZorb marker due to complications with implanted devices. The agency identified this as a Class I recall, the most serious type of recall. Details issued in a written notice by the FDA on May 22 and are shared here.

Hologic incDrug administrationZorb markerBiozorb markerFocal therapeuticsImportant medical device safetyMedwatch adverse event reporting

Dietary Supplement Schwinnng Capsules Recalled For Drugs

Dietary Supplement Schwinnng Capsules is being recalled because it contains Nortadalafil, an active drug, which is illegal.

United statesSchwinnng capsulesMedwatch adverse event reporting

Aruba Aloe Hand Sanitizer Gel Recalled For Undeclared Methanol

Aruba Aloe Hand Sanitizer Gel is being recalled because it contains methanol, which can cause serious adverse health effects.

Aruba generalMedwatch adverse event reporting programAruba aloe hand sanitizer gelAruba aloe alcoholada gelAlcohol madeAruba worldFinest aloeGel pain relievingLidocaine hydrochlorideMedwatch adverse event reporting

FDA Issues Warning on Certain OTC Analgesic Topical Products

FDA warning, medical aesthetics, OTC products, pain medication, topical medication

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