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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
October 8, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/15; Model Numbers: 722058; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859,
Hazard: The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the system will be halted, and the system will not start. No user messages are shown before the battery is low on power or depleted.
October 8, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/10; Model Numbers: 722029; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859,
Hazard: The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the system will be halted, and the system will not start. No user messages are shown before the battery is low on power or depleted.
October 8, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 OR Table; Model Numbers: (1) 722015, (2) 722023, (3) 722035; Associated 510(k)s: K102005, K130638, K1
Hazard: The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the system will be halted, and the system will not start. No user messages are shown before the battery is low on power or depleted.
October 8, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 Biplane OR Table; Model Numbers: (1) 722020, (2) 722025; Associated 510(k)s: K102005, K130638, K13084
Hazard: The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the system will be halted, and the system will not start. No user messages are shown before the battery is low on power or depleted.
October 8, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 Biplane; Model Numbers: (1) 722008, (2) 722013; Associated 510(k)s: K102005, K130638, K130842, K13329
Hazard: The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the system will be halted, and the system will not start. No user messages are shown before the battery is low on power or depleted.
October 8, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20; Model Numbers: (1) 722006, (2) 722012, (3) 722028; Associated 510(k)s: K102005, K130638, K130842, K1
Hazard: The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the system will be halted, and the system will not start. No user messages are shown before the battery is low on power or depleted.
October 8, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10 OR Table; Model Numbers: 722033; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K16
Hazard: The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the system will be halted, and the system will not start. No user messages are shown before the battery is low on power or depleted.
October 8, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10/10; Model Numbers: (1) 722005, (2) 722011, (3) 722027; Associated 510(k)s: K102005, K130638, K130842,
Hazard: The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the system will be halted, and the system will not start. No user messages are shown before the battery is low on power or depleted.
October 8, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10; Model Numbers: (1) 722003, (2) 722010, (3) 722026; Associated 510(k)s: K102005, K130638, K130842, K1
Hazard: The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the system will be halted, and the system will not start. No user messages are shown before the battery is low on power or depleted.
October 8, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10C; Model Number: 722001; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K16
Hazard: The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the system will be halted, and the system will not start. No user messages are shown before the battery is low on power or depleted.
October 8, 2025Food & BeverageFDA
GOOT ESSA, LLC recalls Goot Essa, Der Mutterschaf Cheese, Sheep Tomme Style. 4 and 8 OZ. ( Pasteurized Sheep Milk, Salt, Vegetable Enzymes, Ch
Hazard: The firm had a positive Listeria Monocytogenes on a sample from this batch of product made.
October 8, 2025Food & BeverageFDA
Chefs Warehouse recalls 98 cs Cucumber - Super 6 Ct
Hazard: Product is contaminated with Salmonella
October 8, 2025Food & BeverageFDA
Chefs Warehouse recalls 15 lbs. Cucumbers Diced 1/4"
Hazard: Product is contaminated with Salmonella
October 8, 2025Food & BeverageFDA
Chefs Warehouse recalls 5 lbs. Cucumber Diced 1/2"
Hazard: Product is contaminated with Salmonella
October 8, 2025Food & BeverageFDA
Chefs Warehouse recalls 10lbs. Cucumbers Sliced 1/4", 5 lbs. Cucumber Sliced 1/4"
Hazard: Product is contaminated with Salmonella
October 8, 2025Food & BeverageFDA
Chefs Warehouse recalls 190 cs Cucumber Select 15ct
Hazard: Product is contaminated with Salmonella
October 8, 2025Food & BeverageFDA
Stanley Pearlman Enterprises, Inc. recalls NAFCO, WHITING FILLET SKIN-ON BONELESS IQF, 2 lb., Cases are corrugate. The product is individually frozen and packed in
Hazard: Recall initiated due to the wrong best by date (1-11-2025) being printed on the retail bag which would imply that these are expired but in truth they are good until 1-11-2027.
October 8, 2025Food & BeverageFDA
Tas Tematic Foods Inc recalls Frozen Raw Easy Peel shrimp, IQF, 2-lb bag, 10 bags/case; Generic Brown cardboard box UPC: 021130123223
Hazard: Product which was on FDA hold for high levels of Nitrofuran was inadvertently distributed.
October 8, 2025Food & BeverageFDA
Lawrence Wholesale LLC recalls 16/25 Frozen Cooked Tail-On Farm Raised Shrimp; 12oz clear plastic retail bag. UPC: 011110649812 51/60 Frozen Cooked Ta
Hazard: Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
October 8, 2025Food & BeverageFDA
Lawrence Wholesale LLC recalls Shrimp Cocktail Bowl; 7oz clear plastic retail packaging. UPC: 011110622952 Shrimp Cocktail Bowl; 17oz clear plastic re
Hazard: Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
October 8, 2025Food & BeverageFDA
Vitalabs, Inc. recalls vitamins B12 dietary supplement Raspberry Flavored sold under the following brand names: 1. Black Girl Vitamins 60 gu
Hazard: Undeclared Peanuts. The firm was notified by their supplier, that the product may contain undeclared peanuts.
October 8, 2025Food & BeverageFDA
Pepsico Inc recalls Lipton Green Tea Citrus. 16.9 ounce PET Bottle. sold as 12pk. Outer case label reads as , "*** Lipton Green Tea Citrus (
Hazard: Undeclared sugar in finished product-primary package does not reflect the product inside bottle.
October 8, 2025Food & BeverageFDA
Gina Marie Bakery LLC recalls Toasted Cherry Biscotti
Hazard: Contains undeclared Red 40
October 8, 2025Food & BeverageFDA
Gina Marie Bakery LLC recalls Vanilla Cookies with Raspberry Peach Jam
Hazard: Undeclared Red 3 and Blue 1
October 8, 2025Food & BeverageFDA
Gina Marie Bakery LLC recalls Toasted Almond & Cherry Biscotti
Hazard: Undeclared Red 40
October 8, 2025Food & BeverageFDA
Gina Marie Bakery LLC recalls Vanilla with Apricot Jam Cookies
Hazard: Undeclared Red 40 and Yellow 6
October 8, 2025Food & BeverageFDA
Gina Marie Bakery LLC recalls Vanilla Chocolate Dipped Cookies
Hazard: Undeclared Red 40
October 8, 2025Food & BeverageFDA
Gina Marie Bakery LLC recalls Italian Sesame Cookies
Hazard: Undeclared Sesame, Undeclared Yellow 5, Red 40, Yellow 6
October 8, 2025Food & BeverageFDA
Gina Marie Bakery LLC recalls Italian Mixed Vanilla Cookies
Hazard: Undeclared Almonds, Sesame, Red 40, Red 3, and Blue 1
October 8, 2025Food & BeverageFDA
WFM Purchasing, LP recalls Whole Foods Market Blueberry Almond Granola, PLU 86032, packaged in a clear plastic container.
Hazard: Product was incorrectly labeled, resulting in undeclared wheat, sesame, and cashew.