Check your cabinets: White rice recalled in 13 states FDA issued an update to the recall The Independent UK · Aug 30
Federal Officials Close the Infant Formula Botulism Investigation After Four Babies Were Hospitalized in Three States CDC closed the Nara Organics infant botulism investigation with four hospitalized babies and named a supplier link to a 2025 formula outbreak. Medical Daily · Aug 30
Cyclospora Outbreak Tied to Recalled Lettuce Adds Georgia, Tennessee, and Texas as Confirmed Illnesses Reach 11,458 CDC added Georgia, Tennessee, and Texas to the Taylor Farms lettuce Cyclospora outbreak, now at 11,458 illnesses and 495 hospitalizations. Medical Daily · Aug 30
Why Does It Feel Like Everything Is Being Recalled in 2026? It is hard to walk down the supermarket aisle lately without wondering if anything in your cart is safe. From fresh produce and soft cheeses to eggs and packaged snacks, the steady stream of headlines regarding Salmonella, E. coli, and multi-state contamination warnings makes it feel like the entire food… Grocery Coupon Guide · Aug 30
Cipla Pharma license cancellation: FDA withdraws order after HC raps it for going 'overboard' Maharashtra FDA withdrew its order to cancel Cipla Pharma's drug sale license after court intervention. The Bombay High Court criticized the regulator for acting in a high-handed and overboard manner. The FDA will now issue a fresh show cause notice to the company for a reasoned order. This action followed… The Economic Times · Aug 29
FDA buckles under HC heat, revives Mumbai Cricket Association's suspended eateries after fresh inspection The Bombay High Court warned food officials, leading to a license suspension withdrawal. Restaurants on Mumbai Cricket Association premises will now reopen their services. A recent inspection confirmed 88 percent compliance with food safety rules. The court criticized the FDA for a pedantic rather than pragmatic view. Officials faced potential… The Economic Times · Aug 29
Mounjaro Can Now Be Prescribed to Lower Heart Attack and Stroke Risk in Adults with Type 2 Diabetes FDA approved Mounjaro to lower the risk of heart attack, stroke, and cardiovascular death in adults with type 2 diabetes at high risk. Medical Daily · Aug 29
A Generic Ivermectin Just Became the Fourteenth Emergency Screwworm Drug, and Supply Concentration Is the Reason Why The FDA authorized a generic ivermectin injection for New World screwworm, citing the risk of producers becoming dependent on a single manufacturer. Medical Daily · Aug 29
Baxter Recalls Three Intravenous Solutions on the Same Day Over Fiberglass and Stainless Steel Particle Concerns Baxter recalled three IV solutions due to possible fiberglass and stainless steel particles. Here are the lots, the states, and who is affected. Medical Daily · Aug 28
A Lung Cancer Drug Triggered Pancreatitis That Her CT Scan Could Not See Her pancreatic enzymes were sky-high, and her scans were clean. Doctors traced it to afatinib, weeks after US generics reached the market. Medical Daily · Aug 28
Nineteen Operating Tables Recalled Over a Lock Failure That Could Let a Patient Shift During Surgery The FDA issued recalls for IMRIS ORT200 and ORT300 operating tables due to a rotational lock fault. Surgeons are told to test tables daily. Medical Daily · Aug 28
Juul gets OK to sell updated vaping device with age-gating technology E-cigarette maker Juul Labs has received U.S. permission to sell an updated version of its vaping device The Independent UK · Aug 28
Eli Lilly’s Mounjaro wins FDA approval for a major new cardiovascular benefit Eli Lilly's Mounjaro received FDA approval for reducing heart attack and stroke risks. This new indication expands its use beyond diabetes and weight management. The drug demonstrated an 8% greater reduction in cardiovascular events in a key study. Mounjaro's approval strengthens Eli Lilly's position in the GLP-1 medicine market. This… The Economic Times · Aug 28
The FDA just approved this year’s Covid vaccines - here’s what you need to know about the shots The vaccines are expected to roll out at hospitals and pharmacies in just days The Independent UK · Aug 28
Bored Panda · Aug 28 New Cancer Med Is Giving Patients Hope, But One Former Senator Says It Comes With A “Nasty” Catch The FDA has approved a new cancer treatment. It's a tablet meant to help patients with pancreatic cancer. But the side-effects can be brutal, and visually shocking, despite its success rate. The full story is in the article.
The Economic Times · Aug 28 Tukaram Mundhe cracks down: Maharashtra FDA cancels licence of Cipla's Pune unit over regulatory violations, Cipla contests action Maharashtra FDA cancelled Cipla's Pune C&F unit drug sale licenses due to serious storage and recall issues. Inspectors found unauthorized claims on Reactin Plus Tablets packaging and seized stock valued at over eleven lakh rupees. The company failed to fully comply with market recall directions and address further distribution system…
Medical Daily · Aug 28 Fresenius Recalls 1,140 Dialysis Machines Over Alarms That Can Force Patients Onto Backup Equipment During Treatment FDA posted a recall of 1,140 Fresenius 2008T BlueStar dialysis machines over flow, water, and temperature alarms. What patients should ask.
Medical Daily · Aug 28 Federal Regulators Give Their Most Serious Recall Label to Morphine Syringes That May Contain a Stronger Opioid FDA labeled the Fresenius Kabi morphine syringe recall as Class I. Lot 6402820 may contain Dilaudid instead. Here is what patients should know.
The Guardian - US · Aug 28 ‘So much fringe science’: RFK Jr’s advisers are pushing an extreme makeover in autism research Experts warn the 336-page plan from RFK Jr’s advisers deflects federal dollars into unreliable alternative therapies
Medical Daily · Aug 28 Federal Investigators Trace Wellness Clinic IV Reactions to a Single Ingredient Lot Used by Multiple Compounding Pharmacies FDA links at least 30 IV glutathione reactions to one supplier lot. Here is what patients at med spas and wellness clinics should check.
International Business Times UK · Aug 28 Natalie Harp's Cancer Story Questioned After Claiming Trump Law Saved Her Despite Taking Treatment Before It Natalie Harp's cancer survival story, linked to Trump's Right to Try Act, faces scrutiny over timeline discrepancies and medical claims.
Medical Daily · Aug 28 Federal Officials Close the Requeson Listeria Investigation with 15 Illnesses and a Final Case Reported in July FDA and CDC closed the Clover Hill Dairy Listeria investigation with 15 cases and one death. Frozen cheese remains the open household risk.
Medical Daily · Aug 28 A Once Daily Pill Becomes the First Approved Treatment for Dermatomyositis After Decades of Borrowed Therapies FDA approved Lisraya (brepocitinib), the first oral drug indicated for dermatomyositis. Here is the trial evidence, the boxed warning, and the cost.
Medical Daily · Aug 28 Regulators Flag 184 Serious Injuries Tied to a Swallowed Capsule Used in Routine Acid Reflux Testing FDA issued an early alert on Medtronic Bravo CF capsule delivery devices after 184 serious injuries. Here is what reflux patients should ask.
Medical Daily · Aug 28 Updated COVID Shots Matched to the XFG Variant Reach Pharmacies While Federal Eligibility Guidance Remains Unsettled FDA approved updated 2026-2027 COVID vaccines targeting XFG. Here is who qualifies, what insurance covers, and what guidance is still missing.