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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21451–21475 of 39673

  • SevereNHTSA·17V070000·2017-02-03

    Volkswagen Recalls 2017 Jetta Vehicles Due to Engine Seizure Risk

    Volkswagen is recalling 2017 Jetta vehicles with 1.4L engines because the engine block may be improperly cast, potentially causing the engine to seize and leading to a loss of vehicle control.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V072000·2017-02-03

    REV Recalls 2016-2017 Motorhomes Due to Fuel Leak Risk

    REV Recreation Group is recalling 391 Holiday Rambler and Fleetwood motorhomes because a spring shackle bolt may puncture fuel components, creating a fire hazard.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD VACATIONER XE, STORM, VACATIONER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·17V068000·2017-02-02

    Nissan Recalls 2002 Pathfinder and Infiniti QX4 for Air Bag Defect

    Nissan is recalling 2002 Pathfinder and Infiniti QX4 vehicles because the front passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    INFINITI — INFINITI, NISSAN QX4, PATHFINDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17081·2017-02-02

    Disney Recalls Mickey Mouse Nightlights Due to Fire Hazard

    Walt Disney Parks and Resorts is recalling Happy Holidays! Mickey Mouse Nightlights because liquid can leak onto electrical outlets, posing a fire hazard.

    Product
    Happy Holidays! Mickey Mouse Nightlights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V067000·2017-02-02

    BMW Recalls 2011-2012 Models for Rear Driveshaft CV Joint Defect

    BMW is recalling specific 2011-2012 models because the rear driveshaft CV joint may break, causing loss of propulsion and increasing crash risk.

    Product
    BMW — BMW 335I, Z4, 335D, 535I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1299-2017·2017-02-01

    Dutch-American Foods Recalls Natural Ranch Seasoning Due to Salmonella Risk

    Dutch-American Foods Inc is recalling Natural Ranch Seasoning due to potential Salmonella contamination. The product was distributed in Maryland, Michigan, Illinois, and Florida.

    Product
    Natural Ranch Seasoning, NET Wt. 50 lbs (22.73kg)
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-1375-2017·2017-02-01

    Jem Cashew Masala Tahini Recalled Due to Confirmed Salmonella

    Jem Raw Chocolate LLC is recalling Cashew Masala Tahini in 16 oz, 6 oz, and 1.27 oz jars due to a confirmed positive test for Salmonella.

    Product
    Cashew Masala Tahini, Jem brand, 16 oz glass jar has UPC 8 61437 00037 3. Cashew Masala Tahini, Jem brand, 6 oz glass jar has UPC 8 61437 00034 2. Cashew Masala Tahini, Jem brand, 1.27 oz glass jar has UPC 8 61437 00033 5.
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-1300-2017·2017-02-01

    Dutch-American Foods Recalls Truco Nacho Seasoning for Salmonella Risk

    Dutch-American Foods is recalling Truco Nacho seasoning products due to potential Salmonella contamination. The recall affects 6 bags distributed in Maryland, Michigan, Illinois, and Florida.

    Product
    Truco Nacho, NET Wt. 50 lbs (22.73kg)
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-1361-2017·2017-02-01

    Earth Balance Vegan Mac and Cheese Recalled for Undeclared Milk

    Boulder Brands is recalling Earth Balance Vegan Mac and Cheese products due to undeclared milk, a major allergen.

    Product
    Earth Balance Vegan White Cheddar flavored Mac and Cheese, 6oz package, Cardboard box/carton, 12 packages per distributed case, Ambient storage.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0923-2017·2017-02-01

    Philips Allura Xper FD10 X-ray System Recalled for Loose Screws

    Philips is recalling one Allura Xper FD10 X-ray system because production errors left screws loose, potentially causing the C-arm to rotate uncontrolled.

    Product
    Allura Xper FD10 722026 is intended for: Cardiovascular and vascular X-ray imaging applications, including diagnostic, interventional procedures (such as PTCA, stent placement and atherectomies), pacemaker implantations and Electro Physiology(EP).
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Food)·F-1345-2017·2017-02-01

    SYNEDREX Weight Loss Solution Recalled for Unapproved Ingredients

    IQ Formulations is recalling SYNEDREX weight loss capsules because they contain Picamilon and/or methylpentane citrate, which are not recognized as dietary ingredients.

    Product
    SYNEDREX, Powerful stimulant weight loss solution, 45 capsules (UPC 764779-224592). Brand: Metabolic Nutrition.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1305-2017·2017-02-01

    Dutch-American Foods Recalls White Chocolate Mousse for Salmonella Risk

    Dutch-American Foods is recalling 1-Step White Chocolate Mousse due to potential Salmonella contamination. Consumers in MD, MI, IL, and FL should stop using the product.

    Product
    1-Step White Chocolate Mousse, NET WEIGHT: 1 BAG: 35 oz/ 1 kg
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-1065-2017·2017-02-01

    Villa Radiology Systems Recalls Apollo DRF X-Ray Systems Due to Injury Risk

    Villa Radiology Systems LLC is recalling 66 Apollo DRF multi-function x-ray systems because a chain of faults led to an injury involving inadvertent movement activation.

    Product
    Apollo DRF: Model: 9784220831 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.
    Category
    Medical Device
    Distribution
    26 states
  • SevereNHTSA·17V065000·2017-02-01

    Highland Ridge Recalls 2016-2017 Open Range Fifth-Wheels for Axle Defect

    Highland Ridge RV is recalling 2016-2017 Open Range fifth-wheel vehicles because axle hangers may puncture the riser tube, causing axle misalignment and tire failure.

    Product
    HIGHLAND RIDGE FW — HIGHLAND RIDGE FW OPEN RANGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1350-2017·2017-02-01

    IQ Formulations Recalls Pre-Workout Powder Containing Unapproved Ingredients

    IQ Formulations is recalling P.S.P. Pre-Workout powder because it contains Picamilon and/or methylpentane citrate, which are not recognized as dietary ingredients.

    Product
    P.S.P., Pre-Workout, Physique Stimulating Pre-workout, Powder, 360 g, watermelon flavor (UPC 764779-360450). Brand: Metabolic Nutrition
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1303-2017·2017-02-01

    Dutch-American Foods Recalls Creamy Ranch Seasoning for Salmonella Risk

    Dutch-American Foods is recalling Creamy Ranch seasoning products due to potential Salmonella contamination. The recall affects 70 bags distributed in Maryland, Michigan, Illinois, and Florida.

    Product
    Creamy Ranch, Net Wt. 50 lbs (22.73 kg), Item Number 16131505
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1337-2017·2017-02-01

    Victory General Foods Recalls Elder Paintsil's GA Kenkey for Insanitary Conditions

    Victory General Foods is recalling Elder Paintsil's GA Kenkey because it was manufactured under insanitary conditions and without following required food code processes.

    Product
    ELDER PAINTSIL'S GA KENKEY, NET WT. 1.20, UPC: 6 61799 58166 0, MANUFACTURED BY VICTORY GENERAL FOODS IN WORCESTER, MA 01603
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1351-2017·2017-02-01

    Metabolic Nutrition Pre-Workout Powder Recalled for Unapproved Ingredients

    IQ Formulations is recalling Metabolic Nutrition P.S.P. Pre-Workout powder because it contains Picamilon and/or methylpentane citrate, which are not recognized as dietary ingredients.

    Product
    P.S.P., Pre-Workout, Physique Stimulating Pre-workout, Powder, 360 g, blue raspberry (UPC 764779-360122). Brand: Metabolic Nutrition.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1063-2017·2017-02-01

    Villa Radiology Juno DRF X-ray Systems Recalled for Injury Risk

    Villa Radiology Systems LLC is recalling Juno DRF x-ray systems after an injury occurred due to a chain of faults involving physical barriers and labeling.

    Product
    Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.
    Category
    Medical Device
    Distribution
    26 states
  • SevereFDA (Devices)·Z-0925-2017·2017-02-01

    Philips Allura Xper FD20/15 C-arm Recall Due to Loose Screws

    Philips is recalling two Allura Xper FD20/15 systems because production errors may cause C-arm screws to loosen, leading to uncontrolled rotation.

    Product
    Allura Xper FD20/15 R8.2 722058 is intended for: Cardiovascular and vascular X-ray imaging applications, including diagnostic, interventional procedures (such as PTCA, stent placement and atherectomies), pacemaker implantations and Electro Physiology(EP).
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1064-2017·2017-02-01

    Villa Radiology Systems Recalls Apollo X-Ray Systems Due to Injury Risk

    Villa Radiology Systems LLC is recalling 66 Apollo multi-function x-ray systems after an injury incident involving inadvertent movement activation and delayed emergency stop response.

    Product
    Apollo: Models: 9784000131, 9784000231, 9784020131, 9784020231, 9784100231, 9784120131, 9784120231, 9784130131 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.
    Category
    Medical Device
    Distribution
    26 states
  • SevereFDA (Food)·F-1357-2017·2017-02-01

    Berner Creamy Alfredo Pasta Sauce Recalled for Bacterial Contamination

    Berner Food & Beverage is recalling Creamy Alfredo Pasta Sauce contaminated with spoilage bacteria. Consumers should stop using the product.

    Product
    Creamy Alfredo, Pasta Sauce; NET WT. 15 OZ, CONT. NET 425g; Glass jar, metal lid; UPC 41220845941, 70038626695 or 041498172855
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Devices)·Z-0924-2017·2017-02-01

    Philips Allura Xper FD20 C-arm Recall Due to Loose Screws

    Philips is recalling two Allura Xper FD20 C-arm systems because production errors left screws loose, posing a risk of uncontrolled rotation.

    Product
    Allura Xper FD20 R8.2 722028 is intended for: Cardiovascular and vascular X-ray imaging applications, including diagnostic, interventional procedures (such as PTCA, stent placement and atherectomies), pacemaker implantations and Electrophysiology(EP).
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Food)·F-1346-2017·2017-02-01

    IQ Formulations Recalls E.S.P. Pre-Workout Powder for Unapproved Ingredients

    IQ Formulations is recalling E.S.P. Pre-Workout powder because it contains picamilon and/or methylpentane citrate, which are not recognized as dietary ingredients.

    Product
    E.S.P. Pre-Workout, Energy Stimulant Pre-workout, Powder, 300 g, Watermelon flavor (UPC 764779-4407566). Brand: Metabolic Nutrition.
    Category
    Food
    Distribution
    0 states