
‘Fungal Growth On Food, Expired Items': FDA Suspends Zepto's License In Mumbai's Dharavi
Last Updated:
The FDA stated that the suspension will remain in effect until the establishment achieves full compliance and receives clearance from the licensing authority.
The food business licence of quick-commerce unicorn Zepto in Dharavi, Mumbai, has been suspended by the Maharashtra Food and Drug Administration (FDA) for non-compliance with food safety standards.
Following the information received from the Minister of State for FDA, Yogen Kadam, an inspection was conducted which revealed several violations. These included fungal growth on certain food items, improper maintenance of cold storage temperatures, inadequate separation of expired and valid stock, food products stored directly on the floor, wet and dirty floors, and the storage of food items near clogged and stagnant water.
According to the FDA, Kiranakart Technologies, the firm operating Zepto, violated the Food Safety and Standards Act (2006) and the Food Safety and Standards (Licensing and Registration of Food Businesses) Regulations, 2011.
'The findings constitute a failure to comply with the conditions of the licence. Accordingly, Anupamaa Balasaheb Patil, Assistant Commissioner (Food), ordered an immediate suspension under Section 32(3) of the Food Safety and Standards Act, 2006, and Regulation 2.1.8(4) of the Licensing and Registration Regulations, 2011," the FDA said in a statement.
The FDA stated that the suspension will remain in effect until the establishment achieves full compliance and receives clearance from the licensing authority.
There has been no official comment from Zepto. The licence remains invalid until the conditions are met.
Hashtags

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


Time of India
4 hours ago
- Time of India
Entrepreneur finds alternative to make areca plates safer after US ban
Mangaluru: Entrepreneur and researcher Nivedan Nempe has developed an innovative, eco-friendly alternative following the recent US ban on arecanut leaf sheath dinnerware. His intervention comes at a crucial time, as areca growers and industry experts from Karnataka's areca belt have appealed to Prime Minister Narendra Modi to seek the lifting of the restriction. The US Food and Drug Administration (FDA) issued an import alert banning dinnerware made from areca catechu sheaths, citing the presence of naturally occurring toxins that may migrate into food at unsafe levels. The FDA's concerns significantly impacted India's $400-500 million areca plate industry, with nearly 80–85% of exports directed to the US. Most manufacturers are concentrated in Dakshina Kannada and Shivamogga, and the ban threatens the livelihoods of many families. Nivedan, founder of Areca Tea and operating in Udupi and Shivamogga, acknowledged the FDA's concerns and told TOI: "As a preventive step, the FDA banned imports. But this severely affects Indian manufacturers. The Indian industry made efforts, including writing to the FDA, but the industry is at risk." In response, Nempe engineered a food-grade, anti-microbial paper lining that acts as a barrier between the food and the areca plate, preventing toxin migration and fungal growth. "The material is certified, heat-resistant up to 300°C, durable, printable, and gives a premium finish. It meets international safety standards without altering the existing production process," he said. While the innovation may increase production costs by 10–15%, Nivedan believes that it is the best way forward. "Our lab results were positive on all parameters. It even looks better than bagasse plates. My goal is to safeguard the industry and support the farmers by supplying this new food-grade paper."


Mint
10 hours ago
- Mint
Bodor Laser's Global Troubles Mount: U.S. Lawsuit, FDA Recall, and Indian Customs Action Raise Red Flags Over Safety
May 2025 |— Bodor Laser, a laser cutting machine manufacturer that once touted itself as a global leader, is now grappling with mounting regulatory and legal scrutiny across two of the world's largest industrial markets: the United States and India. In the U.S., Bodor is facing a multi-million-dollar wrongful death lawsuit filed in Nevada following the fatal crushing of a 38-year-old worker, Jose Luis Ortiz Rojas, at a manufacturing facility in Las Vegas. The incident involved a Bodor P3015 laser cutting machine, which allegedly failed to detect Ortiz's presence after he opened the side door. Despite the company's promotional claims of 'intelligent visual collision avoidance,' the lawsuit asserts that the machine's safety system was either disabled or nonfunctional at the time of the accident. The plaintiff's family further accuses Bodor of fraudulent marketing practices, arguing that the company misled customers via exaggerated safety claims on its website and in product videos. The civil case has ignited serious concerns among U.S. regulators and industrial buyers, with product liability, gross negligence, and deceptive trade practices forming the core of the legal complaint. Adding regulatory weight to the controversy, the U.S. Food and Drug Administration (FDA) recently issued a Class II recall affecting 269 units of Bodor's P and C Series laser cutting machines produced between 2018 and 2024. The recall notice cited the absence of mandatory interlock systems, lack of presence detection, and improper certification labeling. In 2024, the FDA issued a formal Import Alert, subjecting further shipments to heightened scrutiny or outright refusal of entry into the U.S. market. Bodor has since announced corrective measures, including hardware retrofits and on-site inspections, but the damage to its reputation appears significant. Several U.S.-based metal fabricators are reportedly reassessing their Bodor installations in light of the recall. While Bodor's challenges in the U.S. stem from product safety and regulatory labeling, the company's India operations are now embroiled in a separate, high-stakes customs dispute. In October 2024, Chennai Customs seized three consignments of laser machines imported by Bodor Laser India Pvt. Ltd., citing false declaration of origin. The shipments were listed as 'Made in Thailand,' but inspections revealed substantial Chinese-origin components and packaging — a potential attempt to bypass India's anti-dumping duties on Chinese goods. The seized shipments, valued at ₹ 37.7 million, have not been released. Indian authorities have demanded a provisional bond of ₹ 152 million (roughly USD 1.8 million) to cover potential penalties and duties. The matter is being investigated under Sections 110 and 114A of the Customs Act, and criminal prosecution is reportedly under consideration. When seen together, the U.S. safety violations, FDA recall, and Indian customs seizure suggest a troubling pattern of systemic noncompliance across multiple jurisdictions. Bodor's marketing claims, safety engineering, and trade conduct are all under the microscope. As both developed and emerging markets tighten oversight on imported industrial equipment, Bodor Laser's challenges serve as a high-profile warning to global exporters: regulatory diligence is not optional—it's the price of long-term market access.


Time of India
11 hours ago
- Time of India
US FDA launches AI tool to reduce time taken for scientific reviews
Bengaluru: The U.S. Food and Drug Administration said on Monday that it had launched a generative AI tool , Elsa , aimed at improving efficiency across its operations, including scientific reviews . "Today's rollout of Elsa is ahead of schedule and under budget, thanks to the collaboration of our in-house experts across the centers," said FDA Commissioner Marty Makary. The agency said it is already using Elsa to expedite clinical protocol reviews , shorten the time needed for scientific evaluations, and pinpoint high-priority inspection targets. Once the FDA receives an application for a potential drug approval , it has six to 10 months to make a decision. Elsa assists with reading, writing, and summarizing tasks. It can summarize adverse events to support safety profile assessments of drugs and rapidly compare packaging inserts. "Elsa offers a secure platform for FDA employees to access internal documents while ensuring all information remains within the agency. The models do not train on data submitted by regulated industry, safeguarding the sensitive research and data handled by FDA staff," the FDA said. In May, the regulator said it would fully integrate AI by June 30, following an experimental run.