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The Food and Drug Administration called out Colgate-Palmolive for using water contaminated with dangerous bacteria in its products and failing to address the problem. The FDA sent a warning letter to the brand for what it calls "significant violations" of the CGMP regulations. Specifically, the company's Tom's of Maine, Inc. facility was found to have used water contaminated with multiple bacteria for its oral products between June 2021 and October 2022.  Some of the bacteria found are potentially resistant to antibiotics making it "extremely challenging" to treat. It now requires Tom's of Maine to make a comprehensive assessment of its manufacturing operations and respond within 15 days. Link in bio to find out what types of bacteria were found and which products were affected. #biohackyourself Disclaimer: The information provided here is for entertainment and educational purposes only. It is not intended to substitute medical professional advice, diagnosis, or treatment. Always seek the advice of your physician or another qualified health provider with any questions you may have regarding a medical condition. Visit the disclaimer link for more details: https://lnkd.in/eJE9Rsty

FDA issues warning letters to mushroom and produce importers for critical safety violations By News Desk on November 4, 2024 The Food and Drug Administration sends warning letters to entities under its jurisdiction as part of its enforcement activities. Some letters are not posted for public view until weeks or months after they are sent. Business owners have 15 days to respond to FDA warning letters. Warning letters often are not issued until a company has been given months to years to correct problems. The FDA has issued warning letters to two produce importers, Future Best Trading Inc. and Paso Real Produce LLC, for major violations under the Foreign Supplier Verification Program (FSVP). Both firms received a Form FDA 483a, detailing their serious compliance lapses. https://lnkd.in/gHXRpG_7

FDA issues warning letters to mushroom and produce importers for critical safety violations By News Desk on November 4, 2024 The Food and Drug Administration sends warning letters to entities under its jurisdiction as part of its enforcement activities. Some letters are not posted for public view until weeks or months after they are sent. Business owners have 15 days to respond to FDA warning letters. Warning letters often are not issued until a company has been given months to years to correct problems. The FDA has issued warning letters to two produce importers, Future Best Trading Inc. and Paso Real Produce LLC, for major violations under the Foreign Supplier Verification Program (FSVP). Both firms received a Form FDA 483a, detailing their serious compliance lapses. https://lnkd.in/gHXRpG_7

FDA Poised to Decide the Fate of Controversial Red Dye in Food and Candy https://lnkd.in/gBYKqzWH #ciobulletin #LatestNews #FDADecision #RedDyeControversy #FoodSafety #CandyRegulations #HealthConcerns #ConsumerAwareness #FoodAdditives #DyeDebate #PublicHealth #RegulatoryAction

Dec 6. Time is running out to tell the FDA suggestions on how to improve the nation's food supply. See article for link #Dietitian #media #radio #magazine #contentwriter #counselor #health #wellness

Canada - Modification to the List of Contaminants and other Adulterating Substances in Foods as part of the modernization of Part B of the Food and Drug Regulations https://lnkd.in/dtrCY6ci

Did you know that federal quality standards for bottled water have been in place since 1973?💧Today, bottled water is strictly regulated by FDA, under the Federal Food, Drug, and Cosmetic (FD&C) Act. You can sip conveniently and confidently knowing that—by federal law—the safety and quality regulations for bottled water must meet or exceed the standards set by the Environmental Protection Agency (EPA) for tap water. ✅ In fact, in certain cases, such as lead, bottled water regulations are even more stringent! 💦 #SafetyFirst #StayInformed #StayHydrated Learn more: bit.ly/3N8mJsJ

An FDA inspection led to the discovery of “significant violations” at Tom’s of Maine manufacturing facility, which included infections causing bacteria in water used to make toothpaste and a black “mold-like” substance. The FDA said the brand also used the same water to rinse numerous pieces of equipment. On Nov 5, The Food and Drug Administration (FDA) outlined such violations in a warning letter sent to the parent company Colgate-Palmolive after the agency found disease-causing bacteria and mold-like and powdery substances in its products and facilities. According to the FDA, Tom's responded that it handles complaints with a "risk-based approach" and that individual complaints are not enough to deem a product inadequate. Follow for the latest updates. . . . #FDA #Inspection #Violations #Toothpaste #Safety #Health #Mold #Bacteria #ConsumerSafety #TomsofMaine #Colgate #ProductWarning #FDAInspection #Manufacturing #PublicHealth #Contamination #WaterSafety #QualityControl #HealthRisk #Cleanliness #Regulations #ConsumerAlert #FDAWarning #HealthMatters #News #WorldSpotlightNews

Watch our on-demand webinar with Fabiola C. Negrón, "Are you FDA Ready? Key Requirements and Enforcement for Food Facilities" which provides food manufacturers with a comprehensive overview of FDA food facility requirements and essential tips for FDA readiness! Watch Now: https://hubs.li/Q02RfP_T0 #FoodandBeverage #RegistrarCorp #FDACompliance #FreeWebinar

FDA #Detentions occur when the U.S. Food and Drug Administration holds imported #food products that may violate safety standards. Reasons for detention include #contamination, #mislabeling, or failing to meet regulatory requirements 🛑 🥑 🥕 If a company's products are detained, the firm must act promptly. First, they should review the detention notice to understand the specific violations. Next, they should gather documentation and evidence to demonstrate #compliance with #FDAstandards. This may include lab tests, production records, or third-party certifications. 👉 https://lnkd.in/eggsik7W Engaging with an #FDAcompliance expert can help navigate the process. Companies should respond to the FDA with a detailed corrective action plan, addressing the issues and outlining measures to prevent future violations. Timely and thorough communication is key to resolving detentions and ensuring the swift release of products. #FDA #foodsafety #compliance #importexport #regulations #foodindustry #productsafety #USDA #foodregulations #foodtesting #foodlaboratory Paulina Gastelum Laura Thomas Kevin Lewellyn Jeff Briceño-Castillo Brian McGillivray Justine Jannone Monique Alvarado Dhairya Patel Miguel Valero Ramón Bouza Deaño José Luis Ganivet Mateo José Acosta Llinares Mario Reyes