A previous egg recall has been upgraded to a Class 1. A total of 1,589,577 cartons of eggs are affected and were produced and distributed by Midwest Poultry Services L.P. between June 6 and July 3, 2026, with sell-by or best-by dates ranging from July 20 through August 17, 2026. The cartons contain Julian Date Range 157 to 184, identifying codes P-1950 or 0840962, and one of several UPC codes listed in the initial recall notice.
They were sent to food service and retail customers in six states: Arkansas, Louisiana, Mississippi, New Mexico, Oklahoma, and Texas. A majority of the illnesses have been in Texas.
August 18, 2026 – Dreyer’s Grand Ice Cream, Inc. is voluntarily recalling a limited number of select flavors of Outshine Fruit Bars due to possible foreign material contamination with glass. Products affected include Outshine Strawberry, Watermelon, Grape, Tangerine and Black Cherry 6-Count 2.5 ounce Fruit Bars and the Outshine 24-Count 2.5 ounce Variety Pack Fruit Bars.
No other Outshine products or varieties are impacted. ONLY the five flavors of 6 Count (2.5-oz bars) and Outshine Variety 24-Count (2.5-oz bars) Fruit Bars. Batch codes can be identified on the product packaging.
Hardie’s Fresh Foods Recalls Jalapenos Because of Possible Health Risk
Dairyland Produce, LLC, dba Hardie’s Fresh Foods of Houston, TX and Dallas, TX are recalling PEPPER JALAPENO 5#, because it has the potential to be contaminated with Salmonella
Recall of Jalapeno Avocado Dressing Because of Possible Health Risk
HOUSTON, TX (August 11, 2026) – Salata Dressings of Houston, TX, is recalling its Jalapeno Avocado Dressing because it had the potential to be contaminated with Salmonella
The U.S. Food and Drug Administration (FDA) just upgraded a recent berry recall to its highest health risk level, according to an enforcement report.
In late July, Publix announced a recall of GreenWise organic whole blueberries and mixed berries due to potential Escherichia coli (E. coli) contamination. The FDA has now classified the recall as Class I, which the agency assigns to product recalls “in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.”
Exotique Foods Inc Recalls Momchipz Veggie Chips Broccoli Florets & Cauliflower Due to Undeclared Gluten
August 14, 2026, Exotique Foods Inc in Ontario, Canada is recalling Momchipz Veggie Chips Broccoli Florets & Cauliflower because it may contain undeclared gluten. People who have an allergy or severe sensitivity to gluten run the risk of serious or life-threatening allergic reaction if they consume this product.
Prince Bakery Inc Issues Allergy Alert on Undeclared Milk and Sesame in Prince Bakery Breads
Prince Bakery of Bronx, New York is recalling Prince brand Sesame Italian Bread, Large Italian Bread, Large Sesame French Bread, Long Sesame French Bread and Pan de Manteca Spanish Style Bread because they may contain undeclared sesame or milk. People who have an allergy or severe sensitivity to sesame or milk run the risk of serious or life-threatening allergic reaction if they consume these products.
Updated – Grand Central Bakery Seattle Recalls Potato Sourdough Bread Due to Possible Foreign Object
“On 8/19/2026 Additional Grocery Store ‘Metropolitan Markets’ has been added to update the Posting from 8/13/2026.”
August 19, 2026, Grand Central Bakery of Seattle, WA is recalling loaves of Potato Sourdough bread due to the potential presence of pieces of metal.
The following products are subject to recall and were sold at grocery stores, select restaurants, wholesalers, and four Grand Central Bakery (GCB) Café locations within the Seattle and Tacoma Metro areas in WA on 8/10/2026…
L-Nutra Issues Allergy Alert on Undeclared Tree Nuts in Prolon Brand Apulian Almond & Cocoa Spread
L-Nutra of Culver City, California is recalling Prolon brand Apulian Almond & Cocoa Spread because it contains undeclared cashew, pistachio, and hazelnut. People who have an allergy or severe sensitivity to cashew, pistachio, and/or hazelnut run the risk of serious or life-threatening allergic reaction if they consume this product.
The Hampton Grocers, Inc. recalled 8-ounce bags of its Lacnola Lactation Granola, designed for breastfeeding mothers, after receiving notice that a product from one of its ingredient suppliers tested positive for Salmonella. That product contained organic moringa powder, which was also used in the Lacnola Lactation Granola.
No illnesses have been reported in connection with the granola, but Salmonella can cause serious foodborne illness, and in some cases may even be fatal. Read More –
Shan Distribution Network, Inc., located in Carol Stream, Ill., is recalling approximately 5,084 pounds of frozen Siluriformes breaded Swai fish fillet and stick products because they were produced in the United Arab Emirates, a country that is not eligible to export Siluriformes fish to the United States, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The frozen Siluriformes breaded Swai fish fillet and stick products were produced in December 2025, and have use before dates in June 2027. The following products are subject to recall [view labels]:
Indus Foods, LLC, doing business as Gangothri Foods, an Austin, Tex. firm, is recalling approximately 1,626 pounds of ready-to-eat (RTE) pickled goat and chicken products that were produced without the benefit of inspection.
UPDATED: Oma’s Pride Voluntarily Recalls One Lot of Woof Complete Canine Chicken Recipe (6 Lb Bag) Because of Possible Salmonella Health Risk
“The firm updated the press release on August 17, to clarify that the illnesses occurred only in dogs; NO humans illnesses have been reported to date.”
The U.S. Food and Drug Administration (FDA) announced a recall on approximately 11,960,623 bottles of eye drops sold nationwide due to sterility concerns.
The products being recalled are nine types of Rohto Cooling Eye Drops sold at retail locations across the U.S. Distributed by The Mentholatum Company, the following eye drops are affected, including impacted UPCs, lot codes and expiration dates:
There’s an ongoing recall on a specific type of bladder medication distributed and prescribed nationwide, according to the U.S. Food and Drug Administration (FDA).1 This is due to an impurity issue.
The medication being recalled is 25-milligram, 30-count bottles of mirabegron extended-release tablets manufactured by Zydus Lifesciences. The recalled bottles contain a lot code of “E408618,” an NDC of “70710-1159-3” and the expiration date “11/30/2026.”
The bladder medication, prescribed to treat overactive bladder symptoms, is being recalled due to an out-of-specification test result that confirmed an impurity for the active ingredient mirabegron. Therefore, this recall has been classified as Class II, meaning that taking these pills may cause “temporary or medically reversible adverse health consequences.”
Check your medication, and if you have the recalled product on hand, contact your pharmacy for a refund or replacement. Seek medical attention if you are experiencing any health concerns after consuming the affected pills.
Optimal Balance Pharmacy Issues Voluntary Nationwide Recall of Certain Lots of Compounded Glutathione 200 mg/mL Multi-Dose Vials Due to Elevated Endotoxin Levels
FOR IMMEDIATE RELEASE – August 19, 2026 – Houston, Texas, Optimal Balance Pharmacy is voluntarily recalling one lot of Compounded Glutathione 200 MG/ML 30 ML Multi-Dose Vials to the patient level. The product is being recalled because pharmacy testing identified elevated bacterial endotoxin levels.
The FDA has added three products to this safety alert for a number of supplements produced in Mexico. FDA tested the products and found that they contain toxic yellow oleander. The agency is reminding consumers to avoid these products because they have been tested and found to contain toxic yellow oleander and can cause neurologic, gastrointestinal and cardiovascular adverse health effects that may be severe, or even fatal. FDA continues to investigate the safety of botanical weight loss products on the market by testing for yellow oleander.
Additionally, two of these products contain other hidden drug ingredients and may cause life-threatening reactions. See FDA’s notifications for D Magic Plus and B. Magi for more information.
FDA analysis has determined that certain products labeled as tejocote (Crataegus mexicana) root or Brazil seed are adulterated because they contain yellow oleander (Thevetia peruviana) instead of the labeled ingredients. Yellow oleander is a poisonous plant native to Mexico and Central America and a toxic substance of concern to public health officials.
Read entire safety notice for product information
[8-12-2026] The Food and Drug Administration is advising consumers not to purchase or use B. Magi, a product promoted and sold for weight loss on various websites, including www.lamilagrosalab.com, and possibly in some retail stores.
FDA laboratory analysis confirmed that B. Magi contains phenolphthalein, neriifolin and thevetin B not listed on the product label.
Phenolphthalein is a chemical that is not an active ingredient in any approved drug in the U.S. Studies suggest it may increase the risk of cancer.
Neriifolin and thevetin B are found in the yellow oleander (Thevetia peruviana) plant and can cause neurologic, gastrointestinal and cardiovascular adverse health effects that may be severe, or even fatal,
Southern Telecom of Brooklyn, N.Y., is recalling its Brookstone-branded tabletop fire pits due to the risk of serious or fatal burns, according to the U.S. Consumer Product Safety Commission (CPSC).
The company has received two reports of flame jetting and flames escaping from the fire pit’s concrete container, resulting in two injuries, including second- and third-degree burns. Read More –
The U.S. Food and Drug Administration (FDA) has announced a recall of a specific Schwarzkopf product because of a potentially dangerous packaging defect.
On August 11, Henkel Corporation, the owner and manufacturer of the Schwarzkopf brand, stated that it’s voluntarily recalling Schwarzkopf Professional Osis Grip 6.76 fl oz/200 mL, which was sold in the U.S. to both salons and consumers. When the mousse’s can is under pressure, it can leak, and subsequently that leak could cause an explosion. Read recall
Magnetic Building Blocks – Goody King seller Yi Suen Commerce has issued a recall of about 213,500 units of magnetic building toys due to a serious hazard that led to two children needing surgery. A release from the Consumer Product Safety Commission (CPSC) explains that the magnets in the building cubes can become loose if they break or open, making it easy for children to ingest them. This can lead to serious repercussions.
“When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system,” states the CPSC. “This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning, and death.”
