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YOU WONT BELIEVE: 27 - You Need To See This

FDA Moves to Delete Two Food Dye Approvals That Industry Already Stopped Using

FDA finalized revoking Orange B and proposed revoking Citrus Red No. 2. Both were already abandoned by industry, so nothing leaves store shelves.

Medical Daily

Three Injectable Drug Recalls Landed on the Same Day, Including a Widely Used Cancer Drug

Three injectable medicines were recalled July 24, including a chemotherapy drug with steel particles. What patients and caregivers should know.

Medical Daily

Lidl US Expands Recall of Eridanous Shortbread Cookies Over Undeclared Wheat, Soy, Milk, Egg, and Coconut Allergens

Lidl US has expanded a voluntary recall of two varieties of Eridanous Shortbread Cookies due to undeclared allergens, according to an official announcement posted by the U.S. Food and Drug Administration on July 31, 2026.

Grocery Coupon Guide

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Federal Trackers for the Powdered Milk Recall Have Not Been Updated Since May, Even as Agencies Tell Consumers to Check Back

The FDA page tracking the California Dairies recall lists seven downstream recalls and has not changed since May 8. What consumers should still check.

Medical Daily

Moringa Capsules Sold on Amazon Are Recalled After Supplier Testing Flagged Salmonella Before Anyone Got Sick

Zen Principle Moringa Capsules Lot A6FF4 were recalled after FDA testing found Salmonella in the raw powder. No illnesses reported. Check your bottle.

Medical Daily

FDA Reopens Public Comment on BHT, a Preservative Found in Cereal, Frozen Meals and Chewing Gum

FDA reopened its comment period on BHT until August 31 as part of a post-market safety review. Here is what the step does and does not mean.

Medical Daily

Prostate Cancer Patients Just Gained a New Radioligand Option, but Only Licensed Centers Can Give It

FDA expanded Pluvicto to hormone-sensitive metastatic prostate cancer, nearly doubling eligibility. Only licensed nuclear medicine centers can administer it.

Medical Daily

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What Is Retatrutide? The Next-Gen GLP-1 Poised to Become the Most In-Demand Peptide

A deep dive into Retatrutide shows promise—and a lot of danger.

Marie Claire

Patients Waiting Out Drug Shortages Have a Stake in an Obscure FDA Registration Proposal

A quiet FDA rulemaking would require more foreign drug plants to register. Better upstream visibility is how shortages get caught earlier.

Medical Daily

6 Egg Carton Numbers Every Shopper Should Check After the FDA Recall

Recent federal food recalls highlighted serious safety concerns regarding commercial egg packaging. Millions of cartons faced removal from supermarket shelves due to salmonella contamination risks. Shoppers cannot rely solely on visual inspections when purchasing dairy breakfast items. Checking specific carton codes protects your family from dangerous foodborne illnesses. I will…

Grocery Coupon Guide

Hallucinations in Alzheimer's Still Have No Approved Treatment, and the Biggest Trial Program Just Slipped to 2027

Bristol Myers Squibb delayed its Alzheimer's psychosis trial readouts to 2027. Why the treatment gap matters for families managing symptoms now.

Medical Daily

A Breast Cancer Drug Approved on July 14 Was Added to National Treatment Guidelines Sixteen Days Later

Gedatolisib was placed in the NCCN breast cancer guidelines as a preferred Category 1 option 16 days after FDA approval. What does that rating mean?

Medical Daily

A Detroit Health System and Michigan State Just Backed Two Medical Technology Startups, and Neither Product Is Cleared for Sale

Henry Ford Health and Michigan State named the first two investments from their $10M health venture fund. What the technologies do and do not do yet.

Medical Daily

FDA Gives Its Most Serious Recall Class to ResMed Astral Ventilators, but Patients Are Told Not to Stop Using Them

FDA assigned a Class 1 recall to ResMed Astral 100 and 150 ventilators. Patients are told not to stop use. Here is the guidance.

Medical Daily

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Medical Daily

Vaginal Estrogen Is Linked to Fewer Hospitalizations in Women with Repeat UTIs, and Most Eligible Patients Never Fill the Prescription

New database research links vaginal estrogen to lower sepsis and hospitalization rates in women with recurrent UTIs. What the evidence does and does not show.

Medical Daily

FDA Issues Early Alert on ResMed Astral Ventilators as Replacement Parts Run Short

FDA alerts patients that certain ResMed Astral 100 and 150 ventilators may stop therapy. Parts are limited. What families should do now.

Medical Daily

Two New Studies Show More Women Complete Cervical Cancer Screening When Self-Collection Is Offered

Two new studies found that more women completed cervical cancer screening when offered HPV self-collection. Here is where it is authorized in the US.

Reason

Rand Paul's Biosimilar Drug Bill Could Cut Costs, Speed Patient Access

The Expedited Access to Biosimilars Act enables FDA approval of pharmaceutically equivalent biologic medications.

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Medical Daily

A Second B Cell Drug for IgA Nephropathy Was Approved in July and Two More FDA Decisions Are Due by December

FDA approved atacicept for IgA nephropathy in July. Two more drugs face decisions by year's end. Here is what is proven and what is not.

Medical Daily

FDA Sets a Late-2026 Decision on Adding a PARP Inhibitor to Hormone Therapy for Advanced Prostate Cancer

FDA granted priority review to talazoparib plus enzalutamide for HRR-altered metastatic prostate cancer. A decision is expected in late 2026.

Medical Daily

Aquafaba Powder Sold as an Egg Replacement Is Recalled Nationwide Because It May Contain Egg

Rooted in Rare Aquafaba Powder, sold as an egg substitute, is recalled nationwide over undeclared egg. Check the UPCs and best-by dates now.

Medical Daily

Parents Told a Toddler Needs Fillings Under Anesthesia Now Have Trial Evidence for a Drill-Free Option

A trial in 830 children under 6 found that 38% of treated baby teeth showed arrested decay, without drilling or sedation.

Medical Daily

Dead People's Skin Is The Latest Anti-Aging Beauty Craze And It Could Soon Come to the US

A controversial anti-aging injectable made from donated human skin is gaining popularity in South Korea and could reach the US market.

Medical Daily

Public Comment Closes on the FDA Plan to Permanently Bar Bulk Compounding of Semaglutide and Tirzepatide

The comment window on FDA's proposal to keep semaglutide and tirzepatide off the 503B bulk list closed July 30. No final decision has been announced.

Medical Daily

FDA Updates the Testing Rules for the Blood Tubing Used in Every Hemodialysis Session

FDA issued revised final guidance for hemodialysis blood tubing sets, covering kink resistance, sterility, biocompatibility, and the warnings on every label.

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