Latest Product Recalls Today

This recall involves all heating pads and heated blankets sold by JKMax, including models JKMAX-002, JKMAX-7284B, JKMAX-6284B, JKMAX-10090B, JKMAX-8490B and JKMAX-6284B. The heated blankets and heating pads are blue, gray, brown or red. They are made of polyester fabric and are machine washable. The blankets and pads were sold in multiple sizes, and both have a detachable white remote that can be used to adjust the heat. The model number is located on the back of the remote and is also printed on a white label affixed to the product packaging along with the brand name "JKMAX".

This recall involves Jerify Magnetic Humanoid Toys 30 PCS. The 30-piece magnetic toys come in three units of brown, white, green, peach, yellow, pink, blue, orange, purple, and red figures in the shape of a human. Each figure measures about 2.7 inches tall by 2.5 inches wide. The magnetic toys contain magnets in the hand and foot locations. There is no labeling on the product. The magnetic toys come in an unlabeled clear bag enclosed in a brown box with the brand name “Jerify” and number “X003ADA3TD” located on the sticker.

The "Lights and Sound Fire Truck" is a compact fire engine toy with wheels that spin, that also features busy board activities that activate lights and sounds. The toy is made of red plastic, has four black wheels and has a white plastic rotating ladder. The toy has a black plastic connector that looks like a fire hose. The toy measures 10.5 inches high by 14.31 inches wide by 3.06 inches deep and weighs about 1.6 pounds. On the bottom of the toy, "Melissa & Doug" is embossed on the battery compartment box as are two date wheels showing the dates of manufacturer by year and month. Affected units will have one arrow pointing to the number 25 and the second arrow pointing to the number 4 or 5 or they will have one arrow pointing to the number 26 and the second arrow pointing to the number 3. Date codes OET 25100, OET 25150 or OET 26064 are printed on the product packaging of the recalled units.

Editor's Note: This release was updated on September 17, 2026, to add additional states, including Massachusetts, New York, Connecticut, and Illinois, and to remove the specific July 28 import date to more accurately characterize the product as ineligible for import. WASHINGTON, Sept. 09, 2026 , El Eden Import Distributor Corp., a Long Island City, N.Y. firm, is recalling approximately 264 pounds of potato chip products containing chicharrón (pork cracklings) because they were produced in the Republic of Colombia, a country that is not eligible to export meat products to the United States, the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) announced today. The following products are subject to recall [ view labels ]: 45-g. foil bags of “De Todito NATURAL” mixed chips with “CHICHARRÓN AMERICANO JACKS,” “Margarita,” and “NATU CHIPS.” 45-g. foil bags of “De Todito BBQ” mixed chips with “CHICHARRÓN AMERICANO JACKS,” “Margarita,” and “NatuChips.” The products subject to the recall do not bear any import marks on the labels. These items were shipped to a distributor in New Jersey and retail locations in New Jersey, Utah, Massachusetts, New York, Connecticut, and Illinois. Please note, it may be possible as FSIS continues their investigation consignees in additional states may be identified. The problem was discovered when FSIS received a consumer complaint regarding “De Todito” snack products containing dried plantains, potato chips, and chicharrónes, pork cracklings, imported from Colombia, which is ineligible to import any meat or poultry product into the U.S. There have been no confirmed reports of illness or injury due to consumption of these products. Anyone concerned about illness or injury should contact a healthcare provider. FSIS is concerned that some product may be in consumers' pantries. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at  www.fsis.usda.gov/recalls . Consumers and members of the media with questions about the recall can contact Humberto Gallego, Owner, El Eden Import Distributor Corp. at [email protected] . Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to [email protected] . For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/ .

Rewaco Spezialfahrzeuge GmbH (Rewaco) is recalling certain 2024 RF1 ST-3, 2024-2025 PUR3 GT, 2024-2026 RF1 ST-3 Touring, RF1 GT Touring, and PUR3 GT Touring three-wheeled motorcycles. The connection between the piston rod and rod end in the rear shock absorbers may loosen, resulting in a loss of vehicle control. A loss of vehicle control increases the risk of a crash or injury.

Rivian Automotive, LLC (Rivian) is recalling certain 2022-2027 R1S, 2022-2026 R1T, and 2027 R2 vehicles. The rearview camera image may be obstructed by a notification when in reverse. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 111, "Rear Visibility." An obstructed rearview camera image can reduce the driver's view behind the vehicle, increasing the risk of a crash.

Undeclared milk and pecans

Potential E. coli and Salmonella contamination

Undeclared Wheat.

Undeclared allergen (tree nuts): hazelnut, cashew, and pistachio.

The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying.

An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters.

Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

Capsule may fail to attach to the esophagus or detach from the delivery device. Risks include patient aspiration/inhalation, perforation of esophagus, obstruction of the airway, hemorrhage/blood loss/bleeding, laceration of the esophagus, a delay in diagnosis, and foreign bodies remaining in the patient.

Hemodialysis concentrates contain high endotoxin levels

Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.

Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper lidding which may breach the seal area.

Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.

The convenience kits contain .0.9% Sodium Chloride Injection, USP products in Single Dose freeflex bags, which may contain blue Break-off-Parts (BOPs) that have detached from the infusion port during manipulation.

Hemodialysis concentrates contain high endotoxin levels

Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

Hemodialysis concentrates contain high endotoxin levels

An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters.

Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.