Martinelli's recalls 170,000 apple juice bottles over toxic mold risk
California-based S. Martinelli & Co. has issued a voluntary recall of more than 170,000 bottles of its popular apple juice due to concerns over potential contamination with patulin, a toxic substance produced by certain molds that can grow on fruit.
The Watsonville (Santa Cruz County) juice company initiated the recall in March. The Food and Drug Administration classified it as a Class II recall last week, affecting 7,234 cases of 10-ounce glass bottles sold in 4-packs, each with a white metal screw-top lid.
The bottles in question were produced in December 2023 and have a best by date of Dec. 5, 2026. They are marked with UPC number 0 41244 04102 2.
No illnesses have been reported, and the company said all affected products have been removed from store shelves in 28 states, including California.
According to the FDA, patulin is a naturally occurring toxin that may cause nausea, vomiting and gastrointestinal issues. The Class II classification means the product could lead to temporary or medically reversible health effects, though the likelihood of serious harm is low.
'In 2024, the Food & Drug Administration (FDA) routine testing indicated that one lot of 10-ounce Martinelli's Apple Juice glass bottles (in 4-packs only) produced in December 2023 may contain elevated levels of Patulin,' the company said in a statement.
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Through the discovery, development and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Oncology and Inflammation & Autoimmunity. Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe and Asia. For additional information on Incyte, please visit or follow us on social media: LinkedIn, X, Instagram, Facebook, YouTube. Incyte Forward-Looking Statements Except for the historical information set forth herein, the matters set forth in this press release, including statements regarding the potential for ruxolitinib cream to provide a successful treatment option for pediatric patients with AD; Incyte's plans to work with FDA; and Incyte's expectations with regard to the PDUFA date for its sNDA and regulatory approval, contain predictions, estimates, and other forward-looking statements. These forward-looking statements are based on our current expectations and are subject to risks and uncertainties that may cause actual results to differ materially, including unanticipated developments in and risks related to: unanticipated delays; further research and development and the results of clinical trials possibly being unsuccessful or insufficient to meet applicable regulatory standards or warrant continued development; the ability to enroll sufficient numbers of subjects in clinical trials and the ability to enroll subjects in accordance with planned schedules; determinations made by the FDA and other regulatory agencies; the efficacy or safety of our products; the acceptance of our products in the marketplace; market competition; unexpected variations in the demand for our products and the products of our collaboration partners; the effects of announced or unexpected price regulation or limitations on reimbursement or coverage for our products; sales, marketing, manufacturing, and distribution requirements, including our ability to successfully commercialize and build commercial infrastructure for newly approved products and any additional new products that become approved; and other risks detailed from time to time in our reports filed with the U.S. Securities and Exchange Commission, including our annual report on Form 10-K and our quarterly report on Form 10-Q for the quarter ended March 31, 2025. We disclaim any intent or obligation to update these forward-looking statements. View source version on Contacts Media media@ Investors ir@ Error in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data
