Check your freezer ASAP. Tai Foong USA of Seattle, Washington, is recalling its Fusia Asian Inspirations Veggie Spring Rolls because the product contains an undeclared allergen, according to the U.S. Food and Drug Administration (FDA).
The spring rolls may contain shrimp, which is not listed on the packaging. People who have an allergy or severe sensitivity to shrimp or shellfish run the risk of a serious or life-threatening allergic reaction if they consume this product, the FDA warns.
The affected spring rolls were distributed exclusively to Aldi stores nationwide and sold under the Fusia Asian Inspirations brand. They were sold in 10-ounce cardboard boxes with UPC 4099100222258 and a best-before date of 05/17/2027, which is printed on the back panel of the box. The spring rolls are in a vacuum-sealed plastic bag inside the box.
Tai Foong USA discovered that its shrimp spring rolls may have been inadvertently packaged in boxes labeled as vegetable spring rolls. The cause of this labeling error is still being investigated. Aldi has removed the products from its store shelves. Read More –
Ready-to-eat pasta products continue to be recalled in connection with an ongoing Listeria outbreak, according to the U.S. Food and Drug Administration (FDA).
The supplier of the affected pasta, Nate’s Fine Foods, Inc. of Roseville, California, has expanded its recall of certain lots of pre-cooked pasta, including fettuccine, linguine, and farfalle, after a sample of linguine pasta tested positive for Listeria monocytogenes.
In addition to products sold at Walmart and Trader Joe’s stores, the following items have been recently recalled in connection with the Listeria outbreak: Read More –
LSI, Inc. Recalls BBQ Pork Jerky Product Due To Possible Foreign Matter Contamination
Hormel Foods Corporation, an Austin, Minn. establishment, is recalling approximately 4,874,815 pounds of foodservice ready-to-eat frozen chicken products that may be contaminated with pieces of metal, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced.
The affected chicken breast and thigh products were distributed to HRI Commercial Food Service locations nationwide on various dates from February 10, 2025, through September 19, 2025. The following products are subject to recall
More than 2 million pounds of Golden Island Fire-Grilled Korean Barbecue Pork Jerky pouches after people reported finding wiry pieces of metal in the product sold at Costco and Sam’s Club stores nationwide have been recalled, the United States Department of Agriculture announced Friday. Read More –
The following Twin Sisters Creamery cheeses are recalled (the first two cheeses listed were also sold by Peterson Company): Whatcom Blue (with batch code 250527B, 250610B, 250618B or 250624B), Farmhouse (with batch code 250603F or 250616B), Peppercorn (with batch code 250603P) and Mustard Seed (with batch code 250616M) cheeses. Read More –
E.A. Sween Company, an Eden Prairie, Minn. establishment, is recalling approximately 127,887 pounds of a pulled pork sandwich product that may be contaminated with pieces of plastic.
Over 140,000 bottles of Ascend Laboratories’ Atorvastatin Calcium Tablets, a cholesterol medication, have been recalled due to ‘failed dissolution specifications.’ This means the drug may not be absorbed by the body. The recall, classified as Class II, affects various dosages and bottle sizes distributed globally. No illnesses have been reported. Read More
A bladder control supplement sold through Walmart and Amazon has been recalled due to potential contamination with E. coli.
Purity Products recalled one lot of MyBladder, a dietary supplement, sold nationwide through direct delivery from Walmart and Amazon website. Read More –
Nearly 27,000 packs of the birth control pill Viorele have been recalled nationwide, according to the Food and Drug Administration (FDA).1
In early September, Glenmark Pharmaceuticals voluntarily recalled the medication because of “failed impurities/degradation specifications,” which means the birth control may contain unintentional chemical substances or may have broken down from its original form. The affected medication may have issues with safety, quality, or efficacy. Read More –
How FDA recalls work –
A recall may be recommended or requested by FDA or initiated voluntarily at any time by a company. FDA’s role in a recall is to oversee a company’s recall strategy and ensure adequate steps were taken to implement the recall.