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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5276–5300 of 36551

  • SevereUSDA FSIS·043-2023·2023-09-09

    Custom Made Meals Recalls Bacon-Wrapped Chicken Products Due to Undeclared Milk Allergen

    Custom Made Meals, LLC is recalling approximately 1,345 pounds of bacon-wrapped chicken products because they contain undeclared milk, a known allergen.

    Product
    Custom Made Meals, LLC — Custom Made Meals, LLC Recalls Bacon Wrapped Chicken Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V625000·2023-09-08

    2025 Ford E-350 Recalled for Transmission Park Pawl Defect

    Ford is recalling 2025 E-350 trucks and related models due to a transmission park pawl casting defect that may not fully engage, potentially causing vehicle rollaway.

    Product
    FORD — FORD E-350, F-750 SD, F-650 SD, F-650 INCOMPLETE CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V626000·2023-09-08

    Lincoln Aviator and Ford Explorer battery defect poses fire and power-loss risk

    Ford is recalling 2020-2022 Lincoln Aviators and Ford Explorers with 3.0L plug-in hybrid engines. A high-voltage battery manufacturing defect may cause battery failure, loss of drive power, and fire risk.

    Product
    FORD — FORD, LINCOLN EXPLORER, AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V623000·2023-09-07

    2023-2024 Alfa Romeo Tonale plug-in hybrid electric vehicles recalled for fire risk

    Chrysler is recalling 2023-2024 Alfa Romeo Tonale and Dodge Hornet plug-in hybrid electric vehicles. Improperly tightened battery and high voltage connector cables can overheat and cause fires while parked or driving.

    Product
    DODGE — DODGE, ALFA ROMEO HORNET, TONALE, TONALE PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·042-2023·2023-09-07

    USDA Recalls Frozen Pork Products Imported Without Reinspection

    Empacadora Frape, USA LLC is recalling approximately 20,455 pounds of frozen pork chicharron and carnitas that were imported without the required reinspection.

    Product
    Empacadora Frape, USA LLC, Recalls Pork Products Imported Without Benefit of Import Reinspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V624000·2023-09-07

    Midwest Fire Recalls 2022-2023 All-Poly Series Tanker-Pumper Fire Trucks

    Midwest Fire is recalling 2022-2023 All-Poly Series Tanker-Pumper fire trucks due to a software error that may cause a sudden loss of drive power, increasing the risk of a crash.

    Product
    MIDWEST FIRE — MIDWEST FIRE ALL-POLY SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2432-2023·2023-09-06

    Cardiosave Rescue Intra-Aortic Balloon Pumps Fail to Charge When Improperly Inserted

    Datascope Corp. is recalling 9,175 units of Cardiosave Rescue IABP devices because batteries will not charge if the console is not fully inserted into the hospital cart. Users were often unaware of this insertion requirement.

    Product
    Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2431-2023·2023-09-06

    Cardiosave Hybrid Intra-Aortic Balloon Pump charging issue recall

    The Cardiosave Hybrid Intra-Aortic Balloon Pump console fails to charge if not fully inserted into the hospital cart. Users unaware of this requirement may attempt to use a non-charged device during critical cardiac care.

    Product
    Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-UC-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-UC-0800-52, 0998-00-0800-53, 0998-UC-0800-53, 0998-00-08
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1476-2023·2023-09-06

    Stonewall Kitchen Peanut Butter Maltballs Recalled for Undeclared Allergens

    Stonewall Kitchen brand Peanut Butter Maltballs (6oz) may contain undeclared peanut, soy, and wheat. Consumers with allergies to these ingredients should not consume this product.

    Product
    Stonewall Kitchen brand Peanut Butter Maltballs packaged in 6oz clear plastic packaging
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-2433-2023·2023-09-06

    Cardiosave Hybrid IABP devices recalled for temperature and pumping function failures

    Datascope is recalling Cardiosave Hybrid intra-aortic balloon pumps due to reported temperature alarms that can cause loss of pumping function or unexpected standby mode. Users have reported these system failures in critical cardiac support devices.

    Product
    Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-UC-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-UC-0800-52, 0998-00-0800-53, 0998-UC-0800-53, 0998-00-08
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2434-2023·2023-09-06

    Cardiosave Rescue IABP Pumps Recalled for System Overheating and Pump Failure

    Datascope Corp. is recalling Cardiosave Rescue Intra-Aortic Balloon Pumps due to system overheating alarms that can cause loss of pumping function and device shutdown.

    Product
    Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85, 0998-UC-0800-75, 0998-UC-0800-83, 0998-UC-0800-85,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V620000·2023-09-06

    Ducati Recalls 2018-2020 XDiavel Motorcycles for Side Stand Bracket Failure

    Ducati is recalling 2018-2020 XDiavel and XDiavel S motorcycles because a side stand bracket may fail, causing the stand to open while riding and shutting down the engine.

    Product
    DUCATI — DUCATI XDIAVEL S, XDIAVEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2436-2023·2023-09-06

    Cardiosave Rescue IABP Alarms May Trigger Unexpectedly During Therapy

    Datascope Corp. is recalling approximately 9,175 Cardiosave Rescue IABPs because unexpected gas-loss and gas-gain alarms may occur during therapy due to patient movement, blood in the circuit, and hardware issues.

    Product
    Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2438-2023·2023-09-06

    Cardiosave Rescue Intra-Aortic Balloon Pumps Recalled Due to Autofill Failure

    Datascope Corp. is recalling 9,175 Cardiosave Rescue Intra-Aortic Balloon Pumps due to autofill failures that can cause the pump to stop.

    Product
    Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2437-2023·2023-09-06

    Cardiosave Hybrid Intra-Aortic Balloon Pumps recalled for autofill failure

    Datascope Corp. is recalling Cardiosave Hybrid intra-aortic balloon pumps due to autofill failure causing pump stops. The FDA Class I recall affects approximately 9,175 units distributed nationwide.

    Product
    Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-UC-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-UC-0800-52, 0998-00-0800-53, 0998-UC-0800-53, 0998-00-08
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1150-2023·2023-09-06

    Vegetal Vigra Capsules Recalled for Containing Unapproved Sildenafil

    The FDA is recalling Vegetal Vigra 200mg capsules nationwide because they contain sildenafil, an active ingredient in FDA-approved medications. The product was marketed without FDA approval.

    Product
    Vegetal Vigra, 200mg capsules, 8-count bottle, Manufacturer: Hand-shaking (Int'l) Corp. USA ADD: Hand-shaking Mansion, the 5th Ave., Stanford, USA. UPC 8 931028 556885
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2435-2023·2023-09-06

    Intra-Aortic Balloon Pumps recalled for unexpected gas loss and gain alarms

    Datascope's Cardiosave Hybrid Intra-Aortic Balloon Pumps may trigger unexpected alarms indicating gas loss or gain due to undocumented causes including patient movement and blood in the circuit. The FDA Class I recall affects 9,175 units.

    Product
    Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-UC-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-UC-0800-52, 0998-00-0800-53, 0998-UC-0800-53, 0998-00-08
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2467-2023·2023-09-06

    EVIS EXERA III Duodenovideoscope Recalled Due to Patient Infection Reports

    Olympus Corporation recalls 6,426 units of the EVIS EXERA III Duodenovideoscope (Model TJF-Q190V) due to recent reports of patient infections. The device was distributed nationwide in the United States.

    Product
    EVIS EXERA III DUODENOVIDEOSCOPE OLYMPUS TJF-Q190V
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·041-2023·2023-09-05

    AJC International Recalls Frozen Raw Pork Imported Without Reinspection

    AJC International is recalling approximately 17,428 pounds of frozen raw pork products that were imported into the United States without undergoing required reinspection.

    Product
    AJC International, Inc. Recalls Frozen, Raw Pork Products Imported Without Benefit of Import Reinspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·23V617000·2023-09-05

    Peterbilt and Kenworth trucks recalled for fuel hose production defects

    Remote Stage 2 fuel filter hoses in 2023-2024 Peterbilt and Kenworth trucks may be damaged, risking disconnection, engine stall, and fuel leaks that could cause fire or crashes.

    Product
    KENWORTH — KENWORTH, PETERBILT T280, T380, 536, 537
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V616000·2023-09-05

    PACCAR Recalls 2023 Kenworth and Peterbilt Trucks for Driveshaft Defect

    PACCAR is recalling 2023 Kenworth K270, K370, and Peterbilt 220 trucks because the driveshafts can break under certain loading conditions, increasing the risk of a crash.

    Product
    KENWORTH — KENWORTH, PETERBILT K270, K370, 220
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V618000·2023-09-05

    Wilson Recalls One 2024 DWH-750 Trailer for Tire Pressure Loss

    Wilson Trailer Company is recalling one 2024 DWH-750 Pacesetter Grain trailer because the tire pressure regulation system may fail at speeds over 45 mph, increasing crash risk.

    Product
    WILSON — WILSON DWH-750
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·040-2023·2023-09-02

    Banquet Frozen Chicken Strips Recalled for Plastic Contamination

    Conagra Brands is recalling Banquet Chicken Strips Meal due to possible plastic contamination that caused an oral injury.

    Product
    Conagra Brands (Conagra Foods Packaged Foods, LLC) — ConAgra Brands Inc. Recalls Banquet Brand Frozen Chicken Strips Entree Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·039-2023·2023-09-02

    Hillshire Brands Recalls Smoked Sausage Due to Bone Fragments

    Hillshire Brands is recalling smoked sausage products due to possible bone fragment contamination. One oral injury has been reported.

    Product
    The Hillshire Brands Company — Hillshire Brands Company Recalls Smoked Sausage Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    7 states
  • SevereNHTSA·23V613000·2023-09-01

    Audi Recalls 2023 E-Tron GT Models for Battery Fire Risk

    Audi is recalling 2023 RS E-Tron GT and E-Tron GT vehicles because insufficient battery sealant may allow liquid accumulation, increasing the risk of electrical arcing and fire.

    Product
    AUDI — AUDI RS E-TRON GT, E TRON GT
    Category
    Vehicle
    Distribution
    Distributed nationwide