
Urgent recall issued for popular ice cream brand for plastic contamination fears
Wells Enterprises has recalled 22 varieties of its three-gallon tubs of frozen desserts that went to 103 distribution centers across the US.
The company based in Le Mars, Iowa, initiated the voluntary recall on April 25. But the US Food and Drug Administration (FDA), which is a federal agency protecting public health across the nation, on May 14 upgraded the recall to Class II, which is the second-highest level for products.
Anywhere from 17 to more than 5,000 tubs of each item are under the recall. Wells Enterprises makes ice cream for popular brands including Blue Bunny and Glenview Farms.
Many of the affected items are vanilla flavored.
The item that is most impacted is Vanilla Frozen Yogurt, which has 5,280 tubs under the recall. It is followed by Glenview Farms Artificially Flavored French Vanilla Ice Cream with 2,261 tubs recalled, BIPC Flavored Ice Cream with 1,858 tubs recalled, Glenview Farms Vanilla Flavored Ice Cream with 1,573 tubs recalled, and Gordon Choice Vanilla Flavored Ice Cream with 1,080 tubs recalled.
There are also 961 tubs of Vanilla Flavored Ice Cream, 937 tubs of Planet Smoothie ZSA Vanilla Flavored Fat Free Frozen Yogurt, 726 tubs of Scooper Hero Ice Cream, 699 Ellington Farms Vanilla Flavored Ice Cream, and 569 tubs of Keith Valley Vanilla Flavored Ice Cream recalled.
In addition, there are 359 tubs of Mocha Almond Fudge Ice Cream, 320 tubs of Vanilla Bean Ice Cream with Madagascar vanilla, 280 tubs of Quick Blend Vanilla Flavored Ice Cream, 240 tubs of Country Rich Vanilla Ice Cream, and 201 tubs of Peanut Butter 'N Fudge Ice Cream recalled.
The items with a relatively fewer number recalled were Rocky Road Flavored Ice Cream with 169 tubs affected, GFGB Vanilla Bean Flavored Ice Cream with 120 tubs, GFGB 12% Vanilla Flavored Ice Cream with 109 tubs, Johnny Rockets Vanilla Flavored Ice Cream with 100 tubs, Glenview Farms Chocolate Ice Cream with 67 tubs, Cotton Candy Flavored Ice Cream with 39 tubs, and Artificially Flavored French Vanilla Ice Cream with 17 tubs.
They have best if used by dates from March to October 2026.
The FDA defines Class II as the product possibly being able to 'cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote'.
Le Mars was nicknamed the 'Ice Cream Capital of the World' in 1994 just because Wells Enterprises is headquartered there. Items under the recall were produced at the company's South Ice Cream Plant located in Le Mars.
The FDA classification came days after the supermarket chain Publix recalled pouches of baby food over fears of lead contamination.
Get in touch with our news team by emailing us at webnews@metro.co.uk.
For more stories like this, check our news page.
MORE: Urgent recall of macadamia nuts over E.coli contamination fears
MORE: Family 'find wrong man in loved one's casket wearing his suit'
MORE: Joe Biden's 'aggressive' cancer diagnosis: Type, treatments and prognosis
Hashtags

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

Reuters
2 hours ago
- Reuters
American Kratom Association Issues Policy Advisory to State Attorneys General Urging Immediate Crackdown on Dangerous 7-OH Products
WASHINGTON, DC, July 31, 2025 (EZ Newswire) -- Today, American Kratom Association (AKA), opens new tab issued a formal policy advisory to the attorneys general in every state that has enacted a Kratom Consumer Protection Act (KCPA), urging them to take immediate enforcement action against the unlawful sale of highly dangerous 7-hydroxymitragynine (7-OH) products that are misleadingly marketed as kratom. This action comes in response to the recent decision by the U.S. Department of Health and Human Services (HHS) and the U.S. Food and Drug Administration (FDA) to recommend that 7-OH be placed into Schedule I of the Controlled Substances Act, opens new tab, citing overwhelming evidence of its opioid-like effects, high abuse potential, and serious risks to consumer safety. 'Let's be clear: 7-OH is not kratom,' said Mac Haddow, senior fellow on public policy for the American Kratom Association. 'It is a chemically altered, synthetic opioid analogue that hijacks the reputation of natural kratom to sell highly addictive and dangerous products to unsuspecting consumers. These are not traditional botanical kratom products — they are designer opioids with a new label.' 7-OH Sellers Exploiting Public Confusion The urgency of enforcement is amplified by recent reckless and disturbing communications from 7-OH product manufacturers, who are advising distributors not to remove these dangerous products from shelves despite the impending scheduling: "100% no reason to take 7-OH off shelves. Watch sales soar after this. You couldn't buy this kind of advertising!" — leading 7-OH manufacturer This brazen statement shows the callous disregard of bad actors for public health and safety. It is a direct attempt to capitalize on regulatory confusion while putting lives at risk. Every Sale Puts a Consumer at Risk The FDA has confirmed that 7-OH acts as a full mu-opioid receptor agonist, producing effects more potent than morphine, including respiratory depression, dependence, withdrawal, and overdose. Yet, these products are being marketed and sold over the counter in gas stations, smoke shops, and online platforms under the misleading guise of being kratom. 'Every 7-OH sale is a public health time bomb. Consumers have no idea they're buying a synthetic opioid, and the consequences can be fatal,' said Haddow. 'State attorneys general must act immediately to enforce existing laws under the KCPA and remove these products from the market.' KCPA Provides the Legal Tools While several states have enacted the KCPA, products that exceed safe 7-OH thresholds — or contain synthetically derived 7-OH — are explicitly illegal based on consumer protection laws designed to protect consumers from marketing deception. The AKA advisory urges attorneys general to use their statutory authority to: Federal Action Must Be Reinforced at the State Level With the DEA now considering the FDA's scheduling recommendation, state action is more important than ever to protect consumers in the interim period. 'The FDA has done its job. Now it's time for state enforcement agencies to do theirs. We are calling on every attorney general to step up and protect their citizens before any life is lost,' concluded Haddow. About American Kratom Association (AKA) American Kratom Association (AKA) is a consumer-based, nonprofit organization, focused on furthering the latest science as guidance for kratom public policy. AKA works to give a voice to millions of Americans by fighting to protect their rights to access safe and natural kratom. For more information, visit and learn more at Media Contact Mac Haddowmhaddow@ ### SOURCE: American Kratom Association (AKA) Copyright 2025 EZ Newswire See release on EZ Newswire


Metro
2 hours ago
- Metro
Urgent warning over energy drink cans mistakenly filled with vodka
An energy drink company has been forced to recall some of its drinks after the cans were accidentally filled with alcohol. Celsius is recalling certain batches of its Astro Vibe Sparkling Blue Razz Edition energy drink after its cans were mistakenly sent to a vodka seltzer company. The company, High Noon, filled the empty Celsius cans with their alcoholic beverage, and has since also been forced to recall some of its Beach Variety packs which came from the same production line. The US Food and Drug Administration (FDA) put out a warning message warning customers not to drink the product if it features the affected lot codes on the bottom of the cans. They advise customers to throw away the affected cans, but also said that no illness or adverse reactions had been reported as a result of this recall so far. The FDA said: 'Consumption of the liquid in these cans will result in unintentional alcohol ingestion. 'The recall was initiated after High Noon discovered that a shared packaging supplier mistakenly shipped empty Celsius cans to High Noon. More Trending 'Consumers who have purchased the identified product should contact High Noon consumer relations to get more information on next steps, including refunds.' The recall impacts High Noon Beach Variety 12-packs with the following lot codes on the pack's exterior: L CCC 17JL25 14:00 to L CCC 17JL25 23:59 to L CCC 17JL25 L CCC 18JL25 00:00 to L CCC 18JL25 03:00 It also affects Celsius 12fl oz cans of the Astro Vibe Sparkling Blue Razz Edition energy drink, with the following lot codes lasered onto the bottom of the cans: L CCB 02JL25 2:55 to L CCB 02JL25 3:11 The affected cans all have silver lids instead of black lids, the FDA added. Get in touch with our news team by emailing us at webnews@ For more stories like this, check our news page. MORE: Urgent product recall of Waitrose protein pot over risk of salmonella contamination MORE: Tesco urgently recalls beloved pasta salads over salmonella fears MORE: One killed in Listeria outbreak sparking urgent recall on supermarket ready meals


Daily Mail
7 hours ago
- Daily Mail
FDA upgrades recall of cookie products to most dangerous class... 'reasonable probability of death'
The FDA has upgraded a cookie recall danger classification, designating the risk of eating them as causing 'a reasonable probability of death.' The recall was first issued on July 14th when Jalux Americas, Inc, doing business as found undeclared milk and tree nuts not listed on the ingredients label during an inventory audit. The original recall notice said that 'people who have an allergy or severe sensitivity to milk and/or tree nuts (almond and macadamia nuts) run the risk of serious or life-threatening allergic reaction if they consume these products.' The FDA has recently upgraded the danger rating to Class 1, the highest possible. Milk allergies can range from mild to severe. Mild to moderate reactions can lead to skin reactions, GI issues, sneezing or coughing, or a tingling sensation in the mouth. Severe allergies can be life-threatening, causing difficulty breathing due to wheezing and throat swelling, a sudden and dangerous drop in blood pressure, a rapid pulse, and shock, as a result of organs and tissues not receiving enough oxygen. The products impacted by the recall are sold as L'espoir cookies and Drycapot cookies, which contain undeclared tree nuts. Milk and tree nut allergies are common, affecting about 6million Americans and 4million Americans, respectively. Both typically begin in childhood and can lead to life-threatening anaphylaxis. According to the FDA: 'People who have an allergy or severe sensitivity to milk and/or tree nuts (almond and macadamia nuts) run the risk of serious or life-threatening allergic reaction if they consume these products.' The recalled products were distributed in California, Illinois, and Washington and sold exclusively at stores in Torrance, CA; San Jose, CA; Arlington Heights, IL; and Lynnwood, WA. The L'espoir, with undeclared milk, was sold at stores between May 26 and June 30, 2025, and the Drycapot, containing undeclared tree nuts, was sold at stores between May 31 and June 30, 2025. There were no online sales. Jalux Americas, Inc, said: 'The recall was initiated after it was discovered during an inventory audit that L'espoir product containing Milk and the Drycapot product containing Tree Nuts were inadvertently distributed in packaging that did not reveal the presence of those allergens. 'No illnesses have been reported to date.' Consumers who have purchased L'espoir L4FN and Drycapot D4FN products with the best before date of September 26, 2025 should return them to where they bought them for a full refund, the company added. The company has already taken remedial steps, telling Newsweek: 'As part of our preventive measures, our supplier partner has added a step at their manufacturing facility to verify that the product matches the label after it is applied, and to record this verification in the production log. 'Our supplier partner will also reinforce allergy and manufacturing procedure training at the facility. The Drycapot, containing undeclared tree nuts, was sold at stores between May 31 and June 30, 2025 'At the retail store level, we will strengthen our checks during stocking to ensure there are no discrepancies between products and labels, not just for the manufacturer of the recalled products but across all items.' Recalls due to undeclared allergens are not uncommon. Last week, the FDA announced that Tropicale Foods is recalling various Helados Mexico and La Michoacana ice cream products due to undeclared milk, posing a risk of severe allergic reactions. Although 'cream' is listed in ingredients, 'milk' is not explicitly declared, violating allergen labeling laws. And about three weeks ago, the FDA classified a recall by Weaver Nut Company as a dangerous Class 1. Certain chocolate products were recalled due to undeclared milk allergens. The recall was triggered after a customer complaint, and testing confirmed that the chocolate contained milk that was not listed on the ingredients list.