Thousands of gallons of ice cream, frozen yogurt recalled over possible plastic contamination
Wells Enterprises, Inc., the maker of Blue Bunny and other ice cream brands, has issued a voluntary recall of 19 varieties of its 3-gallon ice cream tubs due to the possible presence of plastic material in the products.
The recall, initiated on April 25, affects more than 103 distribution centers across the United States. While no injuries or adverse health effects have been reported, the Food and Drug Administration classified the recall as Class II, meaning the products may cause temporary or medically reversible adverse health consequences.
The affected products include popular flavors such as Rocky Road, Mocha Almond Fudge, Cotton Candy, Peanut Butter 'N Fudge, and several variations of vanilla ice cream and frozen yogurt. They were distributed under various brand names, including Glenview Farms, Gordon Choice, Johnny Rockets, and Planet Smoothie.
The products affected by the recall include:
Rocky Road Flavored Ice Cream — 169 tubs
Mocha Almond Fudge Ice Cream — 359 tubs
Peanut Butter 'N Fudge Ice Cream — 201 tubs
Country Rich Vanilla Ice Cream — 240 tubs
Scooper Hero Ice Cream — 726 tubs
Cotton Candy Flavored Ice Cream — 39 tubs
GFGB Vanilla Bean Flavored Ice Cream — 120 tubs
Quick Blend Vanilla Flavored Ice Cream — 280 tubs
Planet Smoothie ZSA Vanilla Fat-Free Frozen Yogurt — 937 tubs
Johnny Rockets Vanilla Flavored Ice Cream — 100 tubs
BIPC Flavored Ice Cream — 1,858 tubs
Vanilla Frozen Yogurt — 5,280 tubs
Vanilla Flavored Ice Cream — 961 tubs
GFGB 12% Vanilla Flavored Ice Cream — 109 tubs
Gordon Choice Vanilla Flavored Ice Cream — 1,080 tubs
Vanilla Bean Ice Cream with Madagascar Vanilla — 320 tubs
Glenview Farms Vanilla Flavored Ice Cream — 1,573 tubs
Glenview Farms Chocolate Ice Cream — 67 tubs
Glenview Farms Artificially Flavored French Vanilla Ice Cream — 2,261 tubs
Artificially Flavored French Vanilla Ice Cream (Sysco) — 17 tubs
Keith Valley Vanilla Flavored Ice Cream — 569 tubs
Ellington Farms Vanilla Flavored Ice Cream — 600 tubs
Each recalled product is marked with a unique Jet Code and 'Best If Used By' date ranging from April 2026 to October 2026.
KTLA reached out to Wells Enterprises, Inc., but didn't receive a comment in time for publication.
Copyright 2025 Nexstar Media, Inc. All rights reserved. This material may not be published, broadcast, rewritten, or redistributed.
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The results of IBI354 lays the foundation for the subsequent development of Innovent's next-generation of bispecific ADCs and dual-payload ADCs, marking a milestone in Innovent's next-generation "IO+ADC" oncology development strategy. The data presented is from a Phase 1/2 clinical study (NCT05636215) aimed at evaluating the safety, tolerability, and preliminary efficacy of IBI354 in participants with advanced solid tumors. As of March 24, 2025, a total of 368 participants with advanced solid tumors were enrolled and received different doses of IBI354 monotherapy, the median follow-up duration was 11.5 months (range: 0.7-19.6), the median treatment duration was 27.0 weeks (range: 3.1-81.3) and 74 (20.1%) pts were still on treatment. The tumor types including 178 with breast cancer, 92 with ovarian cancer, 38 with colorectal cancer, and 60 with other tumors. IBI354 monotherapy demonstrated excellent safety profile The dosage was escalated to 18mg/kg, with no DLT events observed. 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The median overall survival (OS) was immature with events of 3.4%. In ovarian cancer cohort (n=92, treated at 2~12mg/kg, the median prior treatment lines was 3), the cORR was 41.2% and the DCR was 82.0%. In the 12mg/kg Q3W subgroup (n=40), the cORR reached 55.0% and the DCR was 90.0%. In participants with HER2 1+ (n=27), the ORR reached 55.6% and the DCR was 88.9%. As of the data cutoff date, the median follow-up time was 11.9 months, and the median PFS was 7.1 months (95% CI: 5.2−10.8) in 12mg/kg Q3W dose group. The median OS was not mature with events in 14 (34.1%) pts and a 12-month OS rate of 63.9% (95% CI: 45.0−77.8). Professor Qi Zhou, Chief Physician at the Gynecologic Oncology Center of Chongqing University Affiliated Cancer Hospital and the Principal Investigator of the gynecologic oncology cohort study, stated, "The treatment of platinum-resistant recurrent ovarian cancer is difficult and the prognosis is poor, threatening the life and health of women. Extending PFS and OS in platinum-resistant recurrent ovarian cancer patients remains a clinical challenge for gynecological oncologists. ADC drugs provide a new direction for overcoming resistance mechanisms by precisely delivering cytotoxic agents. HER2, as a validated solid tumor target, has made breakthroughs in breast and gastric cancer fields, while the novel ADC drug IBI354 shows broad-spectrum antitumor activity through unique design in HER2 low-expression (IHC 1+) platinum-resistant ovarian cancer. In the Phase 1 study with a dose of 12mg/kg Q3W, IBI354 demonstrated an ORR of 55.0% and DCR of 90.0%, with a median PFS reaching 7.1 months. The safety profile was very good without common severe interstitial lung disease or ocular toxicity seen in other ADCs. These results significantly outperform traditional chemotherapy regimens, suggesting its potential breakthrough efficacy in the platinum-resistant population. The Phase 3 study of IBI354 in platinum-resistant ovarian cancer (HeriCare-Ovarian01) has been initiated, and I am looking forward to the results, as well as the further validation of the long-term benefits for patients receiving IBI354." Doctor Charlotte Rose Lemech from Scientia Clinical Research Ltd, Australia, stated: "Breast cancer is one of the most common malignant tumors among women globally and remains a leading cause of cancer-related deaths. The amplification or overexpression of HER2 (human epidermal growth factor receptor 2) is recognized as a key driver in the development, progression, and metastasis of breast cancer, with approximately 15%-20% of breast cancer patients exhibiting HER2 overexpression. ADCs have become the new standard treatment for later line HER2 positive breast cancer. In this Phase 1 study, IBI354 has demonstrated encouraging efficacy and safety data, achieving high ORR and DCR especially in 9 mg/kg Q3W subgroup. Long term survival was also achieved with the median PFS of 14.1 months. IBI354 also differentiates itself from other HER2 targeted therapies with its safety profile. The incidence of interstitial lung disease was extremely low and most of the hematological toxicity and gastrointestinal adverse events were mild to moderate and can be effectively managed with standard supportive care. This favorable safety profile enhances the clinical application potential of IBI354 and we look forward to IBI354 achieving more breakthroughs in the field of breast cancer treatment." Dr. Hui Zhou, Senior Vice President of Innovent, stated: "With the rapid development of ADC drugs in the field of tumor treatment, Innovent is steadily advancing its strategic layout in the ADC field. At this year's ASCO conference, we update the safety and efficacy data of IBI354 across various advanced solid tumors. 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These statements are not a guarantee of future developments and are subject to risks, uncertainties and other factors, some of which are beyond Innovent's control and are difficult to predict. Consequently, actual results may differ materially from information contained in the forward-looking statements as a result of future changes or developments in our business, Innovent's competitive environment and political, economic, legal and social conditions. Innovent, the Directors and the employees of Innovent assume (a) no obligation to correct or update the forward-looking statements contained in this site; and (b) no liability in the event that any of the forward-looking statements does not materialize or turn out to be incorrect. View original content: SOURCE Innovent Biologics 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
