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Tomato recall hits US: FDA warns products sold in these 3 states may be deadly

Tomato recall hits US: FDA warns products sold in these 3 states may be deadly

Hindustan Times03-06-2025
Two kinds of tomatoes have been taken off the shelves in 14 states in the US because officials fear they might have salmonella, according to the FDA.
The Food and Drug Administration (FDA) initially issued a recall on 2 May, but the situation has since escalated. On 28 May, the agency officially classified it as a Class I recall.
FDA says the affected tomatoes were sold in just three states: Georgia, North Carolina, and South Carolina. That's where the potentially contaminated produce was distributed between 23 April and 28 April under the H&C Farms Label, according to the FDA.
ALSO READ| Tomatoes recalled across 14 US states due to possible salmonella contamination
The tomatoes were packaged and shipped by Williams Farms Repack LLC, a company based in Lodge, South Carolina. While there have been no reported illnesses or deaths as of now, federal officials are urging caution.
'Freezing and drying may prevent the growth of bacteria, but do not kill salmonella,' the FDA explained. 'The bacteria can live for several weeks in dry environments and for several months in wet environments.'
5x6; R4467
6x6; R4467 and R4470
Combo, 25 pound; R4467
4x4, 2-layer; R4467
4x5, 2-layer; R4467
60-count, 2-layer; R4467
60-count, 18 pounds loose; R4467, R4470
XL, 18 pounds loose; R4467
3 count trays; R4467
'The FDA is urging anyone who bought the recalled tomatoes not to eat them and return them to the place of purchase for a full refund, or they can just discard the affected item,' the FDA said.
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Centers for Disease Control and Prevention (CDC) says it's a harmful organism that can trigger diarrhea, fever, and abdominal cramps, usually within 12 to 72 hours of consumption. While most people recover without medical help, 'salmonella can cause serious and fatal infections in children, the elderly, and other people with weakened immune systems.' Pregnant women are also at risk.
'Consumers who ate the affected tomatoes and have symptoms should contact their health care provider to report their symptoms,' the FDA added.
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Is Novo Nordisk facing its 'Nokia moment'? Stock tumbles to $50 from a year-high of $139 amid disruptive rivals and shifting market forces
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Investors had expected continued dominance in the lucrative obesity and diabetes markets, but the downgrade sent an unmistakable warning: growth is slowing, and the competitive landscape is shifting rapidly. Novo Nordisk's blockbuster drugs Wegovy and Ozempic have faced growing headwinds: Compounded versions from U.S. pharmacies —driven by FDA shortages—have eaten into branded sales. —driven by FDA shortages—have eaten into branded sales. Eli Lilly's Zepbound and Mounjaro are gaining prescription share. As of July 2025, Zepbound holds 59% of prescriptions compared to Wegovy's 40%, signaling a material shift in market preference. These trends highlight a dual threat: traditional competition and unregulated compounding pharmacies undermining pricing power. Longtime CEO Lars Fruergaard Jørgensen stepped down on August 7, 2025, passing the reins to Maziar Mike Doustdar. The new CEO faces immediate challenges: stabilizing sales, defending market share, and restoring investor confidence. Market watchers emphasize that leadership changes at such a sensitive moment can either signal a bold strategic pivot or deepen uncertainty, depending on how quickly Doustdar asserts his vision. Novo Nordisk is also navigating U.S. legal scrutiny. A class-action lawsuit claims the company misled investors about competitive risks and overstated growth prospects. Financial institutions are taking note: UBS downgraded NVO to 'neutral' and cut its target price from 600 to 340 Danish kroner, warning that competitive and compounding pressures are 'here to stay.' Market opinion is divided. Some analysts foresee additional downside, while others highlight support near $47.50 as a potential stabilization point. Contributors on Seeking Alpha argue that the sell-off may have priced in worst-case scenarios, leaving room for a measured recovery if Novo's R&D pipeline delivers next-generation weight-loss drugs or accelerates global expansion. 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Today, it's not just a national success story but a global leader in diabetes, obesity, and rare disease treatments. Despite short-term headwinds, Novo Nordisk is pursuing multiple growth avenues: Amycretin – Dual-Action Obesity Drug: Phase 1b/2a trials show 22% average body weight loss over 36 weeks, sparking a ~12% stock bump. CagriSema – Record Weight Loss in Phase III: Achieved 20.4% weight reduction in obese adults and 13.7% in type 2 diabetes patients. Oral Semaglutide & Amycretin: Oral formulations are under U.S. regulatory review, potentially broadening adoption. $2.2B Septerna Partnership: Four programs targeting obesity, type 2 diabetes, and cardiometabolic diseases. Insulin Icodec (Awiqli) – Once-Weekly Insulin: Approved in Canada, EU, and Japan, improving patient adherence. NNC2215 – Glucose-Sensitive 'Smart' Insulin: Adjusts activity based on blood sugar, reducing hypoglycemia risk. Alhemo (Concizumab) – Hemophilia Treatment: FDA-approved July 2025 for A and B types. AI and Rare Disease Expansion: Collaborations with Heartseed, Ventus Therapeutics, and megaTAL platform targeting cardiovascular, MASH, and CKD therapies. These developments suggest Novo's core capabilities remain strong, providing potential long-term catalysts. Not exactly. While Novo Nordisk faces heightened competition, slowing growth, leadership changes, and legal pressures, it retains robust cash flows, a dominant market footprint, and a promising pipeline. Short-term turbulence is clear. Yet a full-scale Nokia-style collapse is unlikely given Novo's strategic assets and global reach. The company is navigating a near-term storm, but its innovation engine and expansion efforts leave the door open for recovery. 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