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 the agency’s own highest classification or reported deaths or serious injuries, 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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4201–4225 of 39749

  • SevereFDA (Drugs)·D-0585-2024·2024-07-10

    RAM IT Horny Goat Weed Dietary Supplement Recalled for Undeclared Sildenafil

    Integrity Products recalls RAM IT Horny Goat Weed dietary supplement capsules nationwide because they contain undeclared sildenafil, a prescription drug not listed on the label.

    Product
    RAM IT, Horny Goat Weed, dietary supplement capsules, 1000 mg, packaged in a box containing a 10-count blister card, Distributed By: Integrity Products, 1710 Fenpark Dr., Fenton, MO 63026
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2250-2024·2024-07-10

    Reusable Patient Return Electrode Recalled Due to Burn Risk

    MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrodes are recalled due to an identified risk of patient burns. Use should be restricted to patients aged 12 or older.

    Product
    Brand Name: MEGADYNE" MEGA SOFT" Dual Reusable Patient Return Electrode Product Name: MEGADYNE" MEGA SOFT" Dual Reusable Patient Return Electrode Model/Catalog Number: 0835 Software Version: N/A Product Description: Reusable Patient Return Electrode, Mega Soft, Dual Cord…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E059000·2024-07-09

    JecoEV Tesla to CCS Charging Adapter Recall for Fire and Shock Risk

    Dongguan Biaoming is recalling JecoEV Tesla to CCS charging adapters sold on Amazon due to missing over-temperature protection and insecure latching, posing fire and electrical shock risks.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:CHARGING:CABLE/CORD:ACCESSORY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V517000·2024-07-09

    2023 to 2024 Mercedes-Benz Sprinter Rear Suspension U-Bolt Recall

    Daimler Vans USA is recalling certain 2023-2024 Mercedes-Benz Sprinter vehicles due to rear suspension U-bolts with reduced strength from improper heat-treatment. The defect can cause the rear axle to shift, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 1500, SPRINTER 2500, SPRINTER 4500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V518000·2024-07-08

    2021-2024 Nova Bus LFS Parking Brake Air Leak Recall

    Nova Bus is recalling 2021-2024 LFS buses due to an air leak in the parking brake valve that can cause unexpected parking brake engagement without activating brake lights, increasing crash risk.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V515000·2024-07-08

    Autocar Recalls 2023-2024 Xpeditor Trucks for Cab Tilt Hinge Pin Defect

    Autocar is recalling 841 2023-2024 Xpeditor trucks because a missing retaining ring on the cab tilt hinge pin could cause the pin to separate, creating a road hazard and increasing crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·020-2024·2024-07-05

    Al-Safa Recalls Frozen Chicken Products Due to Listeria Contamination

    Al-Safa US LLC is recalling approximately 2,010 pounds of frozen ready-to-eat chicken products that may be contaminated with Listeria monocytogenes.

    Product
    Al-Safa US LLC Recalls Frozen Ready-To-Eat Chicken Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1424-2024·2024-07-03

    Pop a Nosh Mixed Munch snacks recalled for undeclared wheat

    AMB FOODS INC is recalling Pop a Nosh Mixed Munch snacks due to undeclared wheat allergen. Approximately 2,100 units distributed in New York contain wheat, which is not labeled on the product.

    Product
    Pop a Nosh Mixed Munch; Regular Flavor; 8oz plastic bag; Potato Chips, Popcorn, Pretzels; UPC 914669941
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-2140-2024·2024-07-03

    Life2000 Ventilator systems recalled due to battery charging failure risk

    The Life2000 Ventilator may fail to charge or experience intermittent charging behavior due to damage to the battery charger dongle. This FDA Class I recall affects approximately 2,510 units distributed nationwide.

    Product
    Life2000 Ventilator, Product Code: MS-01-0118, which is contained in the Life2000 Ventilator System, with Product Codes BT-20-0002, BT-20-0002A and BT-20-0002AP. The Life2000 ventilation system includes the Life2000 ventilator which has its individual label.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V509000·2024-07-03

    2025 Freightliner and Western Star Steering Tie Rod Assembly Defect

    Certain 2025 Freightliner and Western Star commercial vehicles may have improperly heat-treated tie rod assemblies that can fail, potentially causing loss of steering control and increasing crash risk.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 47X, CASCADIA, 49X, 114SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1389-2024·2024-07-03

    Andersen & Sons Macadamia Nuts Recalled for Listeria Monocytogenes

    Andersen & Sons Shelling, Inc. is recalling its macadamia nuts due to Listeria monocytogenes contamination. Approximately 2,850 pounds were distributed in the United States.

    Product
    Andersen & Sons Shelling, Inc. Macadamia Nuts, Dry Roasted Style 6 25 lbs.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2164-2024·2024-07-03

    Philips MR Torso Coil Recall: Potential Patient Burn Risk

    Philips is recalling 307 SENSE XL TORSO COIL 3.0T units used in MR imaging systems worldwide due to potential for coils to overheat and cause patient burn injuries.

    Product
    SENSE XL TORSO COIL 3.0T. 16-element receive only coil for torso and abdomen imaging in Philips MR Intera and Achieva Systems. Model Numbers: 453567394941, 453567394942, 453567394943, 453567394945, 459801593182. Coils may be included in kits with Mode Numbers: 989603050641…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2159-2024·2024-07-03

    Inspire Model 3028 Implantable Pulse Generator Manufacturing Defect

    Inspire Medical Systems recalls the Model 3028 Implantable Pulse Generator due to a manufacturing defect causing electrical leakage and system malfunction that requires revision surgery. The recall affects 24 devices distributed in the US and Germany.

    Product
    Inspire Model 3028, IV Implantable Pulse Generator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1390-2024·2024-07-03

    Tejocote Root Products Recalled for Yellow Oleander Contamination

    GLOBAL MIX INC. is recalling Tejocote Root Products sold under multiple brand names because they contain Yellow Oleander, a toxic plant. Consumers should not use these products.

    Product
    Tejocote Root Products under the following brands: Eva Nutrition, Science of Alpha Mexican, NWL Nutra Mexican, and Niwali Mexican
    Category
    Food
    Distribution
    42 states
  • SevereFDA (Food)·F-1391-2024·2024-07-03

    ELV Control Herbal Supplement Recalled for Containing Toxic Yellow Oleander

    ELV Control Herbal Supplement is being recalled because it contains yellow oleander instead of the labeled tejocote ingredient. Yellow oleander is toxic to humans. The product was distributed through authorized dealers and e-commerce platforms.

    Product
    ELV Control Herbal Supplement; 90 Capsules
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1425-2024·2024-07-03

    Pop a Nosh Mixed Munch Snack Recalled for Undeclared Wheat Allergen

    Pop a Nosh Mixed Munch in Honey BBQ flavor is recalled due to undeclared wheat allergen. Approximately 2,100 units distributed in New York may lack proper allergen labeling.

    Product
    Pop a Nosh Mixed Munch; Honey BBQ Flavor; 8oz plastic bag; Potato Chips, Popcorn, Pretzels; UPC 914669941
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2163-2024·2024-07-03

    Philips SENSE XL TORSO COIL Recall Due to Potential Patient Burn Hazard

    Philips is recalling SENSE XL TORSO COIL units used in MRI imaging because the coils may heat up excessively and cause patient burns. This FDA Class I recall affects 729 units distributed worldwide.

    Product
    SENSE XL TORSO COIL 1.5T. 16-element receive only coil for torso and abdomen imaging in Philips MR Intera and Achieva Systems. Model Numbers: 453567141882, 453567141883. Coils may be included in kits with Mode Numbers: 989603014351 & 989603014352.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1418-2024·2024-07-03

    Queso Chonero White Cheese Recalled for Listeria Contamination

    Queso Chonero Special White Cheese has been recalled due to Listeria monocytogenes contamination. The product was distributed in Illinois.

    Product
    Queso Chonero Special White Cheese UPC 7 861105 900496
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2165-2024·2024-07-03

    Philips SENSE XL Torso Coil 1.5T Recalled for Overheating Risk

    Philips recalled 14 SENSE XL Torso Coils worldwide due to potential overheating. The coils could heat up during use and cause patient burn injuries.

    Product
    SENSE XL TORSO COIL 1.5T Mk2. 16-element receive only coil for torso and abdomen imaging in Philips MR Intera and Achieva Systems. Model Numbers: 453567502281, 453567502282, 453567502283, 453567502284, 453567502285, 453567502286, 459801585212.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V513000·2024-07-03

    BMW Recalls 3 Series Vehicles Due to Air Bag Inflator Defect

    BMW is recalling 2006-2012 3 Series vehicles because a steering wheel air bag inflator may explode during deployment, posing a risk of serious injury.

    Product
    BMW — BMW 328I, 323I, 335XI, 335I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1422-2024·2024-07-03

    Green Life Farms Baby Arugula Recalled for Salmonella Contamination

    Green Life Farms Baby Arugula in 4.5 ounce clamshells has been recalled due to potential Salmonella contamination. The affected product has lot number LW15124 and a sell-by date of 6/15/24, distributed in Florida.

    Product
    Green Life Farms Baby Arugula in 4.5 ounce plastic clamshell packaging containers. 6 packages per case of 4.5oz each. Store in refrigerator.
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·24V504000·2024-07-02

    Mack Trucks Recalls 2025 Models Due to Tie Rod Assembly Defect

    Mack Trucks is recalling 2025 LR, Granite, and Pinnacle vehicles because a tie rod assembly ball stud may fail, creating a road hazard and increasing crash risk.

    Product
    MACK — MACK PIONEER PR (4), GRANITE (GR), LR
    Category
    Vehicle
    Distribution
    Distributed nationwide