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MYSTERIOUS: 2 - You Need To See This

FDA Halts Shipments from an Indian Plant That Supplied Sildenafil and Tadalafil to U.S. Compounding Pharmacies

FDA inspectors found residue, corrosion, and open-toed sandals at a Gujarat plant supplying U.S. compounding pharmacies. Shipments are halted.

Medical Daily

Texas and New York Are Putting Anti-Choking Devices in Schools While FDA Still Urges Back Blows First

States are stocking schools with suction anti-choking devices. FDA says established rescue protocols come first, and evidence for the devices is thin.

Medical Daily

Peach and Watermelon Vuse Pods Reach U.S. Stores Without FDA Authorization Raising Fresh Youth Access Concerns

Reynolds American is selling four new flavored Vuse Pro pods the FDA never authorized. What the enforcement shift means for parents and teens.

Medical Daily

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Two Weeks into a GLP-1 Diabetes Shot, His Family Noticed a Smell That Stopped When the Drug Did

A 57-year-old man developed an unpleasant body odor on dulaglutide. It faded when he stopped and returned when doctors gave it again.

Medical Daily

Can a New Weight Loss Treatment Escape the Legal and Regulatory Thicket?

It’s Eli Lilly vs. RFK Jr. in a battle over the rules around retatrutide.

Reason

Weight Loss Drug Prescriptions for Children Aged Eight to Eleven Rose Sharply but Remain Rare Nationally

A new Pediatrics study found GLP-1 prescribing in children aged 8 to 11 rose 310-fold since 2019, though only 0.6 percent ever received one.

Medical Daily

Dr. Sarah Daccarett on the Estradiol Patch Shortage and the Delivery Route That Isn't Affected

Women across the United States are being told their estradiol patches are unavailable. The Food and Drug Administration says there is no shortage. Both statements are, in a narrow sense, accurate, and the space between them is where patients are losing access to treatment.

Medical Daily

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HHS Names Permanent Leaders of FDA Drug and Vaccine Centers, Setting the Direction for Future Reviews

HHS has named permanent directors for the FDA centers that regulate drugs, vaccines, and tobacco, plus a first deputy commissioner for AI.

Medical Daily

The First Robot Cleared to Draw Blood on Its Own Will Not Reach US Patients Anytime Soon

The FDA cleared the first autonomous blood draw robot, but Aletta will not reach US patients until a new multicenter trial is done.

Medical Daily

Mumbai ISKCON Govinda's Restaurant licence suspended after FDA finds pest infestation, raw materials not cleaned before cooking

Mumbai’s FDA has suspended the licence of ISKCON’s Govinda’s Restaurant after an inspection found pest infestation, uncleaned raw materials, poor drainage and other food safety and hygiene violations. The FDA also suspended licences of two other food establishments at ISKCON’s Hare Krishna Land in Juhu.

The Economic Times

Erectile Dysfunction Drug Ingredients Sent to Compounding Pharmacies Recalled After Inspectors Found Filth at Indian Plant

FDA found filth and unverifiable test records at a plant supplying sildenafil and tadalafil to US compounding pharmacies. All its ingredients were recalled.

Medical Daily

A New Pancreatic Cancer Pill Lists at $39,800 a Month, and What Patients Actually Owe Varies Widely

Rasonque lists at about $477,600 a year. Here is what Medicare and commercially insured patients may actually pay for the new pancreatic cancer pill.

Medical Daily

Azelaic Acid Is the Most Underrated Ingredient for Brown Skin and Hyperpigmentation in India

What Azelaic Acid Actually DoesAzelaic acid is a dicarboxylic acid that occurs naturally in grains like wheat, rye, and barley. Your skin already encounters trace amounts of it. At the 10 to 20% concentrations used in skincare formulations, it does three distinct things: it inhibits tyrosinase (the enzyme that triggers…

Times Life

Chicken Salad Sandwiches Recalled in Georgia and Florida After Egg Was Left Off the Allergen Statement

FreshPoint recalled 1,093 Created Fresh cranberry chicken salad sandwiches sold in Georgia and Florida. Egg was missing from the Contains statement.

Medical Daily

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Medical Daily

Two Dog Supplements Sold on Amazon and Chewy Are Recalled Over Salmonella That Can Also Sicken People

Fi recalled two dog supplement lots over possible Salmonella. People can get sick from handling the product or pet waste. Lot numbers and next steps.

The Independent UK

Dog supplements sold on Amazon and Chewy recalled over possible contamination

Two supplements from the same company are part of the recall

Medical Daily

Federal Regulators Classify a Sleep Apnea Machine Firmware Recall as Class I After 196 Units Went Uncorrected

FDA classified a BMC Luna G3 APAP firmware recall as Class I. Up to 196 machines may still run the defective version. What users should check.

The Economic Times

Dog supplements sold on Amazon and Chewy in the US recalled over possible salmonella contamination

Two dog supplements have been recalled in the United States for potential salmonella contamination. The recall affects specific lot numbers of Fi Calming and Fi 8-in-1 Formula supplements. Owners are advised to stop using these products and dispose of them safely. Salmonella can affect both pets and humans, with symptoms…

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Medical Daily

Nine Greens and Superfood Powders Recalled Over Salmonella Are Still Sitting in Pantries a Month Later

A Salmonella recall covering nine Food To Live greens powders has resurfaced in FDA enforcement records. The pouches have long shelf lives.

Medical Daily

Late Stage Trial Miss Leaves Adults with Myotonic Dystrophy Still Waiting for a First Approved Treatment

Novartis says its Phase 3 HARBOR trial of del-desiran missed its main goal in myotonic dystrophy type 1, a disease with no approved therapy.

Medical Daily

An Injected COPD Drug Cut Flare Ups About Thirty Percent in Patients Whose Inhalers Were Not Enough

Two Phase III trials of tozorakimab cut moderate and severe COPD flare-ups by roughly 30 percent. An FDA decision is expected in early 2027.

Medical Daily

A One Time CRISPR Infusion for Hereditary Angioedema Now Has a March Decision Date and No Advisory Panel

FDA accepted a priority review for lonvo-z, a one-time CRISPR treatment for hereditary angioedema, with a decision target of March 10, 2027.

Medical Daily

Breast Cancer Drug Wins Accelerated Approval Four Months After FDA Advisers Voted Six to Three Against It

FDA granted camizestrant accelerated approval for ESR1-mutated breast cancer months after its advisory committee voted against the application.

Medical Daily

Compounded Semaglutide and Tirzepatide Have Drawn More Than 1,700 Federal Problem Reports as Peptide Sales Climb

FDA logged 990 reports on compounded semaglutide and more than 730 on tirzepatide through May 31. Here is what buyers should ask.

Medical Daily

Nearly a Year After the FDA Moved to Add a Tylenol Pregnancy Warning the Label Has Not Changed

The FDA said it would change the acetaminophen pregnancy label in September 2025. The current federal label record still shows the old wording.

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