The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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676–700 of 5642

  • SevereFDA (Food)·F-0256-2025·2024-12-11

    Fresh Express Chicken Caesar Salad Bowls Recalled for Listeria Monocytogenes

    Fresh Express Gourmet Cafe Chicken Caesar salad bowls are being recalled due to potential Listeria monocytogenes contamination linked to a Bruce Pac recall. The recall affects products distributed across multiple U.S. states.

    Product
    Fresh Express Gourmet Cafe Chicken Caesar 5.75oz, Labeled Salad Bowls, Refrigerate, UPC Code: 71279407074 and Case Code:071279565620
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Drugs)·D-0083-2025·2024-12-11

    VitalityXtra Capsules Recalled for Undeclared Sildenafil and Diclofenac

    VitalityXtra Capsules containing undeclared sildenafil and diclofenac are being recalled nationwide. The product was marketed without required FDA approval and poses health risks from undeclared pharmaceutical ingredients.

    Product
    VitalityXtra Capsules, 500 mg, packaged in 10 count blisters in cartons, Distributed by: VitalityXtra, San Francisco, CA www.vitalityxtra.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0085-2025·2024-12-11

    ZoomMax Capsules contain undeclared sildenafil and diclofenac

    ZoomMax Capsules have been recalled by the FDA due to containing undeclared sildenafil and diclofenac. The product was marketed without FDA approval.

    Product
    ZoomMax Capsules, 500 mg, 10 count blisters in cartons, Distributed by: ZoomMax, 2108 N St. Sacramento, CA 95816, www.zoommax.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0245-2025·2024-12-11

    Wegmans Asian Sesame Salad recalled for undeclared egg

    Wegmans Large Asian Sesame Salad with Chicken contains undeclared egg, a common allergen. The recall affects 365 units distributed across nine states.

    Product
    Wegmans Large Asian Sesame Salad with Chicken and Asian Peanut Dressing.
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Food)·F-0255-2025·2024-12-11

    Enoki Mushrooms Recalled for Potential Listeria Contamination

    HH Fresh Trading is recalling enoki mushrooms distributed to West Virginia retail stores due to potential Listeria monocytogenes contamination. Consumers should not consume this product.

    Product
    ENOKI MUSHROOM; 200g/package (25 packages/case); vacuum packed; refrigerated "***ENOKI MUSHROOM***Net WT***200g(1.05oz)***To keep sealed & cold Product of Taiwan Distributed by: HH Fresh Trading Los Angeles CA 90063 Exported by JIA YANG INTERNATIONAL ENTERPRISES CO., LTD. Produc
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0257-2025·2024-12-11

    Fresh Express Salad Bowls Recalled for Potential Listeria Contamination

    Fresh Express Gourmet Cafe Santa Fe Greek salad bowls are being recalled due to potential Listeria monocytogenes contamination linked to a chicken ingredient recall. No illnesses have been reported.

    Product
    Fresh Express Gourmet Cafe Santa Fe Greek 5.2 oz, Labeled Salad Bowls, Refrigerate, UPC Code: 71279 40713 5 and Case Code :71279-56704
    Category
    Food
    Distribution
    12 states
  • SevereNHTSA·24V529000·2024-12-07

    2024 Hyundai Santa Fe Transmission Control Software Error Causes Roll-Away Risk

    Hyundai is recalling 2024 Santa Fe vehicles due to a transmission control unit software error that may cause vehicles in PARK to roll away, increasing crash and injury risk. Hyundai will release an over-the-air software update and dealers will inspect and replace the transmission as needed.

    Product
    HYUNDAI — 2024 HYUNDAI SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V531000·2024-12-07

    2025 Forest River Cherokee Travel Trailers Recalled for Hitch Coupler Defect

    Forest River is recalling certain 2025 Cherokee travel trailers with incorrect trailer hitch couplers that may fail when overloaded, increasing the risk of crash or injury.

    Product
    FOREST RIVER — 2025 FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V433000·2024-12-06

    2025 Kenworth and Peterbilt Trucks Steering Linkage Defect

    PACCAR is recalling 2025 Kenworth and Peterbilt trucks due to improperly heat-treated ball studs in steering assemblies that may break, causing loss of steering control.

    Product
    KENWORTH — 2025 KENWORTH W990
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25061·2024-12-05

    Belkin Power Bank Recalls Due to Fire Hazard from Battery Overheat

    Belkin is recalling about 4,000 BoostCharge Pro wireless charger power banks due to a fire hazard from overheating lithium-ion batteries. One unit caught fire and damaged a house.

    Product
    Belkin BoostCharge Pro Fast Wireless Charger Power Banks 10K
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25058·2024-12-05

    NetZero High Bay LED Fixtures Recalled Due to Fire Hazard

    NetZero USA is recalling about 13,000 High Bay LED light fixtures due to plastic pin degradation that can cause the LED board to come loose and catch fire. Seven burning incidents have been reported with no injuries.

    Product
    High Bay LED light fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25056·2024-12-05

    Anker Soundcore and PowerConf Bluetooth speakers recalled for fire hazard

    Anker is recalling about 69,000 Soundcore and PowerConf Bluetooth speakers sold on Amazon in 2023 due to overheating lithium-ion batteries. The firm received 33 reports of incidents, including fires and one minor burn injury.

    Product
    Anker Soundcore (A3102) and PowerConf Bluetooth (A3302) Speakers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0216-2025·2024-12-04

    Atwater's Spider Web Tarts Recalled for Undeclared Almonds

    One Roof LLC recalls Atwater's Spider Web Tarts for undeclared almonds. Consumers with tree nut allergies should not consume this product.

    Product
    Atwater's Spider Web Tarts, 26 tarts packaged individually, 5.73 in x 5.95 in x 3 in clear plastic clamshell container, Julienne date 292
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0148-2025·2024-12-04

    Onion Soup and Dip Mix Recalled for Undeclared Egg Allergen

    Bowl & Basket onion soup and dip mix is being recalled for containing undeclared egg allergen. The product was distributed to one customer in New Jersey. The manufacturer, Gilster-Mary Lee Corporation, initiated the recall voluntarily.

    Product
    Bowl & Basket onion soup and dip mix, net wt 2 oz (2-1oz pouches), UPC 041190083947, Distributed by: Wakefern Food Corp, 5000 Riverside Drive, Keasbey, NJ 08832
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·23V289000·2024-12-04

    2022 Forest River Columbus fifth wheel: missing riser tube risks tire damage and crashes

    Forest River is recalling approximately 137 2022 Columbus fifth wheel vehicles because the riser tube between the axle hangers was not installed. This creates inadequate tire clearance, risking tire puncture and vehicle crashes.

    Product
    FOREST RIVER — 2022 FOREST RIVER COLUMBUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0328-2025·2024-12-04

    Hologic BioZorb Radiographic Marker Recalled Due to Serious Injury Reports

    Hologic has recalled 12,710 BioZorb Markers nationwide after receiving reports of serious complications including infection, device migration, and device erosion. The FDA classified this as a Class I recall.

    Product
    BioZorb Marker. Radiographic soft tissue marker.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V198000·2024-12-03

    2023 Ford Edge child restraint system tether welds insufficient

    Ford is recalling certain 2023 Edge vehicles because child seat tether welds may be insufficient, potentially reducing proper child restraint during a crash. Dealers will replace the seat back frame free of charge.

    Product
    FORD — 2023 FORD EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V121000·2024-12-02

    Thor Motor Coach recreational vehicles recalled for detaching overhead cabinets

    Thor Motor Coach is recalling 2018-2021 Windsport and Hurricane recreational vehicles because the driver and front passenger overhead cabinets may detach while in motion, risking injury to occupants.

    Product
    THOR MOTOR COACH — 2021 THOR MOTOR COACH WINDSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V128000·2024-12-02

    2023 Ford Expedition front axle may fracture, increasing crash risk

    Ford is recalling certain 2023 Expeditions, along with F-150 and Lincoln Navigator vehicles, due to a front axle pinion defect that may not have been properly heat-treated. The defect can cause fracture, loss of 4-wheel drive, and wheel lockup, increasing crash risk.

    Product
    FORD — 2023 FORD EXPEDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0382-2025·2024-11-27

    Baxter Peritoneal Dialysis Transfer Sets Recalled for Chemical Exposure

    Baxter Healthcare Corporation is recalling 1,240 units of MiniCap Extended Life PD Transfer Sets (Part Number T5C4484) due to potential exposure to polychlorinated biphenyls and related compounds when used in peritoneal dialysis treatments.

    Product
    Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp EX Short, Part Number T5C4484; use in Peritoneal Dialysis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0217-2025·2024-11-27

    Frozen U-BAKE Apple Pie recalled for undeclared egg allergen

    Grand Central Bakery FRE Co Inc is recalling 150 packages of U-BAKE Apple Pie due to undeclared egg. The product label declares wheat and milk but not egg, posing a serious risk to consumers with egg allergies.

    Product
    U-BAKE Apple Pie, frozen product and packaged in LDPE bag, net wt. 2lbs. 9oz. Made by Grand Central Baking Company. Label declares Wheat and Milk.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-0143-2025·2024-11-27

    Chicken Alfredo Kit Recalled Due to Listeria Contamination

    Joseph Seviroli, LLC is recalling Chicken Alfredo Kit due to potential Listeria monocytogenes contamination in the chicken. The product was distributed across multiple states.

    Product
    Chicken Alfredo Kit
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Food)·F-0219-2025·2024-11-27

    FDA Recalls U-BAKE Frozen Marionberry Pie for Undeclared Egg

    Grand Central Bakery is recalling U-BAKE Marionberry Pie due to undeclared egg, a major allergen not listed on the label. The recall affects 336 packages distributed in Oregon and Washington with expiration dates from February 1 to April 17, 2025.

    Product
    U-BAKE Marionberry Pie, frozen product and packaged in LDPE bag, net wt. 2lbs. 4oz. Made by Grand Central Baking Company. Label declares Wheat and Milk.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0378-2025·2024-11-27

    Baxter MiniCap Peritoneal Dialysis Transfer Set recalled for potential PCB exposure

    Baxter Healthcare is recalling 58,680 units of its MiniCap Extended Life PD Transfer Set due to potential exposure to polychlorinated biphenyls (PCBs). Users should stop using affected units and consult their healthcare provider.

    Product
    Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482E; use in Peritoneal Dialysis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0218-2025·2024-11-27

    Frozen Pie Crust and Bulk Dough Recalled for Undeclared Egg

    Grand Central Bakery is recalling U-BAKE frozen pie crust and bulk pie dough because they contain undeclared egg. The recall affects products distributed in Oregon and Washington.

    Product
    U-BAKE Pie Crust (Pastry Round), frozen product and packaged in LDPE bag, 2-10.5 inch pie crust per package, net wt. 20oz. Made by Grand Central Baking Company. Label declares Wheat and Milk. Bulk pie dough rolls, packaged in plastic wrap and parchment paper, net wt. 10lbs. Mad
    Category
    Food
    Distribution
    2 states