FDA RECALL
Brand: Dexcom G7
Product: Continuous Glucose Monitoring System
Issue: Sensors identified as scrap were diverted and sold by third-party
Date: 05/29/2026
More: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/dexcom-uncovers-theft-scrapped-product-notifies-potentially-impacted-users #FDA #recall
Dexcom Uncovers Theft of Scrapped Product, Notifies Potentially Impacted Users

SAN DIEGO – MAY 26, 2026 – DexCom, Inc. (Nasdaq: DXCM), the global leader in glucose biosensing, announced today through ongoing quality and accounting reviews it recently identified certain lots of Dexcom G7 sensors originally designated as scrap and intended for destruction were stolen during the

U.S. Food and Drug Administration

Yikes.
It’s Interesting that they know how to notify the people who have purchased the junk sensors if they were stolen and sold.

Please check your sensors even if you got them from the pharmacy. There was a whole entire investigation last year with the year before by Pro Publica that showed how counterfeit medication ends up with PMBs who then send it to the pharmacy who then sells it us.

“DexCom, Inc. (Nasdaq: DXCM), the global leader in glucose biosensing, announced today through ongoing quality and accounting reviews it recently identified certain lots of Dexcom G7 sensors originally designated as scrap and intended for destruction were stolen during the destruction process, then sold by third parties.” ⬇️

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/dexcom-uncovers-theft-scrapped-product-notifies-potentially-impacted-users

#diabetes #dexcom #FDA #recall (sort of)

Dexcom Uncovers Theft of Scrapped Product, Notifies Potentially Impacted Users

SAN DIEGO – MAY 26, 2026 – DexCom, Inc. (Nasdaq: DXCM), the global leader in glucose biosensing, announced today through ongoing quality and accounting reviews it recently identified certain lots of Dexcom G7 sensors originally designated as scrap and intended for destruction were stolen during the

U.S. Food and Drug Administration
Business

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"The FDA's vaccine advisors voted 8 to 0, with one abstention, in favor of a monovalent XFG vaccine for COVID-19 shots for the 2026-2027 season."

Now will the FDA and HHS follow this recommendation? 🤔

https://www.medpagetoday.com/infectiousdisease/covid19vaccine/121483

#PublicHealth #covid #vaccines #immunizations #FDA

FDA Panel Backs New COVID Vaccines Aimed at Dominant Strain

Panelists favored a monovalent XFG-targeted vaccine

MedpageToday
FDA RECALL
Brand: Better Weather
Product: Fix Elixir 15ml
Issue: Undeclared Mitragynine and Mitragynine Pseudoindoxyl (Kratom)
Date: 05/28/2026
More: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/better-weather-actives-llc-recalls-better-weather-fix-elixir-due-undeclared-mitragynine-and #FDA #recall
Better Weather Actives LLC Recalls Better Weather Fix Elixir Due to Undeclared Mitragynine and Mitragynine Pseudoindoxyl

FOR IMMEDIATE RELEASE – May 28, 2026 – Sheridan, Wyoming. Better Weather Actives LLC is voluntarily recalling ALL lots of Better Weather Fix Elixir 15 ml because the products may contain undeclared Mitragynine and Mitragynine Pseudoindoxyl (MP). MP is a more potent derivative of Mitragynine, or Kra

U.S. Food and Drug Administration
FDA RECALL
Brand: D’Dioses
Product: Fruit popsicles
Issue: May Contain undeclared milk, pecans, pistachios, yellow #5 and red #40
Date: 05/27/2026
More: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/de-dioss-ice-pops-ii-llc-issues-allergy-alert-undeclared-milk-pecans-pistachio-yellow-5-and-red-40 #FDA #recall
DE DIOS’S ICE POPS II LLC Issues Allergy Alert on Undeclared Milk, Pecans, Pistachio, Yellow #5, and Red #40 in Popsicles

PATERSON, N.J. – DE DIOS’S ICE POPS II LLC is voluntarily recalling its 3.7 oz. packages of “popsicles” food treats because they may contain undeclared MILK, YELLOW #5, RED #40, PECANS, AND PISTACHIOS. People who have an allergy or

U.S. Food and Drug Administration
FDA RECALL
Brand: SkinnyDipped
Product: Dark Chocolate Coconut Almond Bites
Issue: May Contain undeclared peanuts
Date: 05/27/2026
More: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bazzini-voluntarily-recalls-certain-lots-skinnydippedr-dark-chocolate-coconut-almond-bites-due #FDA #recall
Bazzini Voluntarily Recalls Certain Lots of SkinnyDipped® Dark Chocolate Coconut Almond Bites Due to Undeclared Peanut Allergen

Bazzini, LLC, of Allentown, PA, a co-manufacturer utilized by SkinnyDipped®, is voluntarily recalling a limited number of cases of SkinnyDipped® Dark Chocolate Coconut Almond Bites, out of an abundance of caution, due to the possible presence of undeclared peanut allergen. People who have allergies

U.S. Food and Drug Administration
CIDRAP Op-Ed: Manufacturing a scandal: What the FDA’s COVID vaccine pediatric death review actually says

CIDRAP
US Capitals

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