Posts by PSM Author
California Boutique Recalls Diet Supplements For Containing Banned Sibutramine
Je Dois L’avoir Boutique is voluntarily recalling all of the 365 Skinny High Intensity Pills and or 365 Skinny Emergency Boutique, 30 day capsules supply to the retail/consumer level. The 365 Skinny High Intensity Pills and 365 Skinny Emergency Boutique have been found to contain Sibutramine which is a controlled substance by the DEA.
[...]August 9, 2021: Save Me Magnets!
There are a lot of ineffective and ridiculous #covidscams out in the world, but this particular scam the FDA found that offers to “cure” COVID-19 with magnets takes the cake. Watch “Save Me Magnets!” to learn about this and other harebrained scams. If you need protection from COVID-19, it’s FREE! Text your zip code to 438829 to find out the nearest place for you to get a free vaccine.
[...]Counterfeit HIV Drug Alert: Gilead Warns of Fake Versions of Biktarvy and Descovy Sold to U.S. Pharmacies
Gilead has alerted potentially impacted pharmacies to investigate the potential for counterfeit or tampered Gilead medication sold by distributors not authorized by Gilead that may be within their recent supply and to remain vigilant to the potential for this to occur in the future. The authenticity and safety of Gilead-branded medicines can only be secure when obtained directly through Gilead’s authorized distributors.
[...]Fentanyl Pill Victims Are Getting Younger. Parents Blame Social Media.
On June 4, 2021, parents and family members gathered in 30 cities around the country to protest social media companies’ inaction on drug sales on their platforms. The protest in Santa Monica focused on Snapchat headquarters.
[...]FDA Alert: Third Dietary Supplement Sold on Amazon Recalled for Containing Prescription Drug Ingredients
On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, eBay and other retailers due to hidden and potentially dangerous drug ingredients. It also encouraged online marketplaces to ensure these products are not sold on their platforms.
[...]FDA Alert: Second Dietary Supplement Recalled for Containing Prescription Drug Ingredients
On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, eBay and other retailers due to hidden and potentially dangerous drug ingredients. It also encouraged online marketplaces to ensure these products are not sold on their platforms.
[...]FDA Alert: Dietary Supplement Recalled for Containing Prescription Drug Ingredients
Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using these drug products.
[...]Medication Testing Makes Drug importation Prohibitively Expensive
Medication Testing Makes Drug importation Prohibitively Expensive Federal legislation requires that any Canadian drug importation program test a “statistically valid sample” of medicines from each imported batch. This means you have to test more than a single dose or package, but to achieve 99.99% confidence and reliability, that you test thousands or sometimes tens of…
[...]ED-Marketed Dietary Supplement Recalled Due to Presence of Prescription Drugs
This recall has been initiated after an FDA laboratory analysis found the product to contain undeclared sildenafil and/or tadalafil. Sildenafil and tadalafil are ingredients in FDA approved products for the treatment of male erectile dysfunction in the family of drugs known as phosphodiesterase (PDE-5) inhibitors. The presence of sildenafil and/or tadalafil in Adam’s Secret Extra Strength products makes them unapproved new drugs for which the safety and efficacy have not been established and therefore subject to recall.
[...]FDA Puts All Mexico-Produced Hand Sanitizers on Import Alert
Under the import alert, alcohol-based hand sanitizers from Mexico offered for import are subject to heightened FDA scrutiny, and FDA staff may detain the shipment. As part of their entry review, FDA staff will consider any specific evidence offered by importers or manufacturers that the hand sanitizers were manufactured according to U.S. current good manufacturing practice requirements. This marks the first time the FDA has issued a countrywide import alert for any category of drug product.
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