
Maharashtra: MLA hostel canteen licence suspended after Shiv Sena MLA assaults staff over ‘stale food'
'….the license granted to your establishment from date 26-06-2024 to legal validity date 27-09-2027 is being suspended with immediate effect. You are further informed that during the license suspension period mentioned in the attached order, you or anyone on your behalf should not buy, sell or distribute food items, if found doing so, you should note that legal action will be taken against you for selling/distributing food items without a valid license as per the provisions of the Food Safety and Standards Act 2006 and the rules/regulations there under,'the order issued on Wednesday by the FDA said.
As a purported video of the assault by Gaikwad surfaced on social media, Gaikwad came under the fire by the the Opposition leader as they raised the matter in the Legislative Council and sought his suspension.
Maharashtra Chief Minister Devendra Fadnavis said Gaikwad's behaviour had tarnished the image of the Legislature, and the Assembly Speaker and Legislative Council Chairman should decide on action against him. Saying that elected representatives should behave 'responsibly', Gaikwad's party leader and Deputy Chief Minister Eknath Shinde said he had reprimanded the MLA.
Meet Shah Sena's MLA Sanjay Gaikwad. Last year he had threatened&announced 11 lakh rupees to anyone who cuts off Sh. Rahul Gandhi's tongue. Now the man is seen beating up a poor helpless canteen worker. But wait no news TV outrage here since its a BJP ally pic.twitter.com/XVwnEzJFSU
— Priyanka Chaturvedi🇮🇳 (@priyankac19) July 9, 2025
In the purported video clip of the incident, Gaikwad, wearing a towel and a vest, is seen confronting the canteen staff over what he claimed was sour dal and spoiled rice. He then repeatedly assaults a canteen employee and tells others not to pay their bills. His supporters, too, are seen assaulting the canteen workers.
No police complaint was filed till evening. However the FDA was immediately swing into the action and conducted the inspection at the canteen.
The slueth of FDA collected samples of food from the MLAs' Hostel canteen and sent them for testing. 'The team collected samples of food like paneer, sauces and dal. These will be sent to the laboratory; the reports are expected in 14 days,' an FDA official said.
However soonafter that, the FDA issued a suspension order to the Ajanta Caterer, the private contractor who runs the canteen under the supervision of the Legislature Secretariat.
Speaking to reporters on Wednesday, Gaikwad claimed that was served stale food in his room. He said he had complained about the quality of food earlier, but no action was taken. 'If such food is being served to an MLA, imagine what the common man must be getting,' said the MLA, who represents Buldhana Assembly constituency.
'I have no regrets over what I did. I am a public representative… when someone fails to understand democratic language, then I have to use this language. I had complained to the authorities on several occasions. I don't regret it and I will repeat it if needed,' he said.
'I had complained about the poor quality of food two or three times. This time, the food was absolutely unacceptable… completely spoiled. I will raise this issue in the ongoing Legislative session,' he said. He also met Assembly Speaker Rahul Narvekar to complain about the quality of food.
'People from all across the state come here; workers and officials come here to eat. The quality of food should be good here as it is a government canteen,' Gaikwad said.

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles


Hindustan Times
2 days ago
- Hindustan Times
RFK Jr.'s Dangerous Attack on mRNA Research
Health and Human Services Secretary Robert F. Kennedy Jr. has halted nearly half a billion dollars in funding for mRNA-based respiratory vaccines—and thereby ended America's leadership research into one of modern medicine's most promising frontiers. That verdict runs counter to the evidence. I've spent more than three decades advancing mRNA research. Testing proves it both safe and transformative in the way we fight disease. My work began in the days of basic RNA biology, and it has reached to seeing my graduate student help design the Moderna Covid vaccine. I've watched these discoveries save millions of lives worldwide. Mr. Kennedy's decision must be reversed. The skepticism many Americans have toward mRNA vaccines is easy to understand. The Covid vaccine rollout came with overconfident and misleading assurances that the shots were entirely without risk and that they would prevent infection and transmission. Those claims, delivered with certainty that wasn't backed up by science, proved false. Worse, public-health authorities and employers coupled those messages with sweeping mandates: Take an experimental vaccine or lose your job, your education and access to public spaces. Rather than seeking informed consent, public leaders deployed misinformation and coercive tactics. Being told one thing, then living through another, left a sense of betrayal that damaged the public's trust in health authorities. Acknowledging those errors is mandatory for restoring our credibility. We need to hold two truths at once: The benefits of the Covid vaccine were oversold and the uncertainties understated—and yet, when the data came in, the mRNA vaccines still proved effective at reducing severe illness and death. Here, the evidence is clear. In large, randomized clinical trials reviewed by the FDA, the first mRNA vaccines from Pfizer and Moderna reduced the risk of symptomatic Covid by about 95%. Real-world data from later surges, including the Delta and Omicron waves, confirmed that vaccinated people were far less likely to be hospitalized or die of the virus. The most-discussed adverse event, myocarditis in young men, was real but extremely rare. In the highest-risk group, males age 12 to 17 after a second dose, the risk was roughly 0.006% to 0.011%, about the same as lifetime odds of being struck by lightning. The vaccines were highly effective, and the benefits outweighed the risks by orders of magnitude. That doesn't diminish the experience of anyone who suffered a complication, but it matters when setting national policy. The mRNA vaccines are among the most promising tools in modern medicine. They offer unmatched speed and adaptability, allowing scientists to design and produce targeted vaccines in weeks instead of years. Their potential extends far beyond respiratory diseases. Researchers are now using mRNA to tackle rare genetic disorders, autoimmune diseases, heart disease and cancers. Early trials of customized mRNA vaccines for pancreatic cancer have shown success rates of 50%, echoing the mid-20th-century leukemia breakthroughs that lifted five-year survival from just 10% to 94%. That leap from near-certain death to near-certain survival shows what sustained investment in medical research can achieve. For more than six decades, the U.S. has led the world in biomedical innovation, thanks in large part to sustained federal investment in basic research. That lead is now at risk, as global rivals are moving aggressively to surpass us. Chinese researchers, along with rapidly advancing biotech hubs in other countries, are shortening clinical trial approvals, boosting investment, and attracting record levels of global capital. If we step back, they will seize this field—forcing the U.S. to depend on foreign-made medicines. Once lost, American leadership may never return. American leadership need not, and should not, embrace mRNA technology uncritically. But the government has a responsibility to drive safe, groundbreaking innovation forward. As a scientist whose education was funded by National Institutes of Health grants, I see this as a social contract with the American people. With strong federal backing and a commitment to rapid, responsible progress, mRNA vaccines can realize their full potential. Mr. Coller is a professor of RNA biology and therapeutics at Johns Hopkins University, founder of the Alliance for mRNA Medicines and a co-founder of Tevard Biosciences.


Hindustan Times
7 days ago
- Hindustan Times
Drug Approvals Hit an FDA Wall
Does Food and Drug Administration Commissioner Marty Makary want to accelerate life-saving drugs as he claims? The agency's recent torpedoing of an immunotherapy shot for advanced melanoma and slow-rolling a treatment for a rare disease raise big questions. The FDA's approval of new drugs has notably slowed this year. Annual novel drug approvals averaged 52 in the first Trump Presidency and 48 under Joe Biden, but there have been only 22 in the first seven months of this year. On current trend that would make 38 for the year. One concern is that regulators are nixing drugs under the false flag of raising scientific standards. A case in point is Replimune's melanoma treatment, which the FDA rejected last month. About a third of patients who hadn't responded to prior immunotherapy showed a strong response to Replimune's in a clinical trial. Tumors shrank in nearly all patients, and responses proved durable over three years. Serious side effects were rare. Oncologists who treated patients in the trial hailed the results. Yet the FDA said the trial was 'not considered to be an adequate and well-controlled clinical investigation that provides substantial evidence of effectiveness.' Its quibble is that the trial lacked a control group. Vinay Prasad, the head of the biologics division, has long criticized such single-arm studies that have no placebo groups. He believes medicines should undergo randomized controlled trials that track patients over longer periods to measure overall survival. Never mind if patients die in the interim. It's unethical to give patients with an advanced deadly disease a treatment that failed to help them as a placebo. Measuring overall survival would also require drug makers to run bigger trials and over longer periods, delaying access to potentially life-saving therapies. Replimune executives said they were blind-sided by the FDA rejection and its shifting post-hoc demands. Leading oncologists lambasted the FDA and urged the agency to reconsider. Replimune's 'results are unpredecented,' Vishal Patel, a dermatology oncologist at George Washington University Cancer Center, wrote to Dr. Makary this month. 'Physicians urgently want and need this agent based on the data they have seen,' University of Iowa oncologist Mohammed Milhem wrote in another letter. 'Indeed, the precedent set by this rejection is likely to halt many aspects of the science and clinical development required to move agents like this into practice in later line disease.' 'The world looks for leadership from the FDA based on rationality, science and evidence,' wrote Melanoma World Society president Axel Hauschild. Doing a randomized controlled trial, he said, 'would be considered as unethical' in his home country of Germany. We criticized Dr. Prasad, who was appointed by Dr. Makary, for using dubious safety risks in an effort to scuttle a gene therapy for Duchenne muscular dystrophy. After a public backlash, the FDA backed down, and Dr. Prasad resigned. Yet Dr. Makary recently brought him back. This followed a StatNews story in which anonymous FDA officials sought to pin the blame for the Replimune rejection on Richard Pazdur, the agency's head of oncology. But Dr. Prasad's shop was directly responsible for the Replimune review and his career staff had supported approval. In any case, the buck stops with Dr. Makary. The finger-pointing and his continued support for Dr. Prasad is creating tremendous uncertainty for pharmaceutical developers. If Dr. Makary really wants to make drug approvals for deadly and rare diseases faster and more flexible, he'd send a signal by ordering the FDA to reconsider Replimune's treatment. *** He'd also green-light Stealth BioTherapeutics' treatment for Barth syndrome, which the bureaucracy is strangling. Barth causes a fatal weakening of the heart, muscles and immune system and afflicts about 150 Americans. It's the sort of rare-disease therapy that Dr. Makary says he wants to bring to market faster. Stealth applied for approval in January 2024, and an FDA advisory committee last autumn found the drug to be effective. But the agency keeps changing its demands and has deployed one excuse after another to delay approval. The agency recently told Stealth to resubmit its application, which would take at least six months to review. Stealth CEO Reenie McCarthy says her company might not survive that long. If the company fails, patients that began receiving the medicine in the trial will lose access, and others may never benefit. Parents of children in Stealth's trial are urging the FDA to approve it. So are Democrats and Republicans in Congress. 'I have lost two boys with Barth syndrome and know firsthand how lethal Barth syndrome is,' Shelley Bowen of South Carolina tells us. Do FDA leaders care? Does Dr. Makary?


Time of India
13-08-2025
- Time of India
Maharashtra junior minister Yogesh Kadam seeks more decision-making powers and access to cabinet meetings
Mumbai: Shiv Sena minister of state (MoS) Yogesh Kadam wants more powers and wants to be invited to attend cabinet meetings when subjects related to his departments are discussed. Kadam, who is the MoS for home, revenue, rural development, panchayati raj, food, civil supplies and consumer protection, and FDA, has written to CM Devendra Fadnavis saying that he should be given more powers, at least for taking decisions in his home district in departments like revenue and FDA. Kadam said in his letter that such powers were given to MoSs in the previous govts from 2009 to 2014 under the Congress-NCP govt and even under the Shiv Sena-BJP govt. You Can Also Check: Mumbai AQI | Weather in Mumbai | Bank Holidays in Mumbai | Public Holidays in Mumbai | Gold Rates Today in Mumbai | Silver Rates Today in Mumbai Kadam said he wants powers in revenue and FDA departments through delegation of power, it is learnt. Kadam made the request in writing to Fadnavis recently. So far, Fadnavis has n'ot given any orders on the delegation of powers between cabinet ministers and MoSs. There are 36 cabinet ministers in the Mahayuti govt and 6 MoSs. Four are from BJP and one each from Sena and NCP. MoSs cannot attend cabinet meetings that take place every week. While Kadam was not available for comment, Sena officials said that in previous govts, MoSs were delegated certain powers by the cabinet ministers, but in the current regime, MoSs hardly have any powers barring replying to questions in the sessions of the state legislature. by Taboola by Taboola Sponsored Links Sponsored Links Promoted Links Promoted Links You May Like Redefine Your Future with a Top Online MBA SRM Online Enquire Now Undo Following allegations that Kadam was allegedly running a dance bar with a licence in his mother's name, the Kadam family recently surrendered the orchestra licence of Savali Bar in Kandivli. Last month, in another instance of differences within the Mahayuti govt, a letter war erupted between the cabinet minister for social justice, Sanjay Shirsat, who belongs to the Shiv Sena, and his junior, the minister of state for the department, Madhuri Misal, who belongs to the BJP. Shirsat, who was in the crosshairs of several controversies, sent a letter to Misal, stating she should not call departmental review meetings without his consent and that such meetings should be held under his chairmanship in the future. Misal responded with a letter in which she stated she was within her rights to call review meetings. "I do not think your prior consent is required before convening such a meeting," her letter said. She also called on Fadnavis on Saturday. Her letter emphasised no decisions were taken or directives issued at the meeting. "Taking decisions is your right as minister. By taking a review meeting, I have not come in the way of your authority. If I have taken any decisions, kindly let me know the incidents and examples," she said. She stated the CM gave ministers the responsibility to oversee the progress of govt programmes over 150 days, which gave her the right to convene a review meeting. Stay updated with the latest local news from your city on Times of India (TOI). Check upcoming bank holidays , public holidays , and current gold rates and silver prices in your area.