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.

Filters

Agency

Category

Minimum severity

Clear filters

3001–3025 of 36537

  • SevereNHTSA·25V040000·2025-01-29

    Toyota and Lexus spiral cable fault can deactivate the driver airbag

    Toyota is recalling certain 2023-2024 Toyota and Lexus vehicles that may have been incorrectly repaired under recall 23V-480, because an insufficiently welded connection can deactivate the driver's airbag.

    Product
    TOYOTA — TOYOTA, LEXUS HIGHLANDER HYBRID, COROLLA CROSS HYBRID, RX, HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0411-2025·2025-01-29

    Trail Mix Recall: Undeclared Milk Allergen in Cal Yee Product

    Cal Yee Farm LLC is recalling Tropical Trail Mix due to undeclared milk, a common allergen. The product was sold at 2 California retail stores and via online/phone orders in California and Pennsylvania.

    Product
    Cal Yee's Tropical Trail Mix - assorted nuts and dried fruits (8-oz, 1-lb, 2-lb, 5-lb plastic bags)
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0418-2025·2025-01-29

    Cal Yee's Dark Chocolate Walnuts Recalled for Undeclared Milk Allergen

    Cal Yee Farm LLC has recalled 8-oz bags of Cal Yee's Dark Chocolate Walnuts because they contain undeclared milk. The product was sold at 2 California retail stores and through online/phone orders in California and Pennsylvania.

    Product
    Cal Yee's Dark Chocolate Walnuts (8-oz plastic bag)
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0420-2025·2025-01-29

    KIRKLAND Signature Smoked Salmon Recalled for Listeria Contamination

    Acme Smoked Fish Corp. is recalling KIRKLAND Signature Smoked Salmon due to Listeria monocytogenes contamination. The product was distributed to retail locations in Florida.

    Product
    KIRKLAND Signature Smoked Salmon NET WT 340 g (12 oz) MUST KEEP REFRIGERATED. INGREDIENTS: Atlantic Salmon (Salmo Salar), Salt, and Natural Hardwood Smoke. Color Added. Distributed by: Costco Wholesale Corporation P.O. Box 34535 Seattle, WA 98124-1535 UPC 0 96619 25697 6
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0412-2025·2025-01-29

    Cal Yee's Cajun Sesame Hot Sticks Recalled for Undeclared Wheat and Soy

    Cal Yee Farm LLC is recalling Cal Yee's Cajun Sesame Hot Sticks (1-lb bags) due to undeclared wheat and soybean oil. The product was sold in California retail stores and through online/phone orders in California and Pennsylvania.

    Product
    Cal Yee's Cajun Sesame Hot Sticks (1-lb plastic bag)
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0415-2025·2025-01-29

    Food recall: Cal Yee Farm Dark Chocolate Apricots for undeclared milk

    Cal Yee Farm is recalling Dark Chocolate Apricots due to undeclared milk. The product was distributed to retail stores and online customers in California and Pennsylvania.

    Product
    Cal Yee Farm Dark Chocolate Apricots (8-oz plastic non-flex container) Cal Yee Farms Dark Chocolate Apricots (8-oz plastic non-flex container)
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0960-2025·2025-01-29

    VDR4 Phasitron Breathing Circuit Recalled for Potential Ventilation Reduction

    Percussionaire Corporation is recalling VDR4 Phasitron breathing circuit models due to a venturi component that may stick and reduce ventilation. This Class I recall affects over 4,700 units worldwide.

    Product
    VDR4 Phasitron Breathing Circuit Models that contain the venturi component: -A50094 D 5PK, Phasitron Kit, VDR, Single Patient, 5pk -A51001, VDR4 Control Unit Tester -PRT 991, VDR W/SWIVEL T SINGLE PATIENT PHASITRON -PRT 992, VDR4 HUMIDIFICATION ADAPTER KIT, CASE OF 10 -PRT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0416-2025·2025-01-29

    Yogurt Coated Almonds Recalled for Undeclared Milk Allergen

    Cal Yee's Yogurt Coated Almonds recalled for undeclared milk. Voluntary recall covers products distributed to retail stores and online/phone orders in California and Pennsylvania.

    Product
    Cal Yee's Yogurt Coated Almonds (8-oz, 1-lb)
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0413-2025·2025-01-29

    Cal Yee's New Orleans Hot Mix Recalled for Undeclared Wheat and Soybean Oil

    Cal Yee's New Orleans Hot Mix contains undeclared wheat and soybean oil. The product was distributed to retail stores in California and through online and phone orders in California and Pennsylvania. Consumers with these allergies should not consume the product.

    Product
    Cal Yee's New Orleans Hot Mix (1-lb plastic bag)
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0207-2025·2025-01-29

    FOUZEE SugarLin Herbal Formula Capsules Recalled for Undeclared Prescription Drugs

    Shoppers-Plaza is recalling FOUZEE SugarLin Herbal Formula capsules because FDA testing found undeclared metformin and glyburide. The product was marketed without FDA approval.

    Product
    FOUZEE SugarLin HERBAL FORMULA capsules, 180 capsules per bottle, Sold and Distributed by Shoppers-Plaza, Hawthorne, CA 90250. Product of India. UPC 8 26656 69047 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0409-2025·2025-01-29

    Dark Chocolate Almonds Recalled for Undeclared Milk Allergen

    Cal Yee's Dark Chocolate Almonds contain undeclared milk and are being recalled. The product was distributed at 2 California retail stores and online in California and Pennsylvania.

    Product
    Cal Yee's Dark Chocolate Almonds (8-oz plastic bag)
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·25V038000·2025-01-28

    Freightliner chassis fuel filter hoses can separate causing leak and stall

    Daimler Trucks is recalling certain 2022-2025 Freightliner Custom Chassis vehicles with Cummins L9 diesel engines because remote fuel filter hoses may separate from the fitting, causing a fuel leak and engine stall.

    Product
    FCCC — FCCC XCM, XCS, XCR, XBS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V037000·2025-01-28

    Mitsubishi Fuso Recalls 2024 Rizon Trucks for Wiring Seal Defect

    Mitsubishi Fuso is recalling 233 2024 Rizon trucks because an improperly sealed chassis harness may allow water intrusion, causing loss of drive power and increasing crash risk.

    Product
    MITSUBISHI FUSO — MITSUBISHI FUSO RIZON FEC7K (E16), RIZON FEC9K (E18)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V013000·2025-01-24

    Ducati Recalls 2025 Panigale V4 S for Rear Brake Hose Heat Damage

    Ducati is recalling 2025 Panigale V4 S motorcycles because excessive heat may damage the rear brake hose, causing sudden brake loss and increasing crash risk.

    Product
    DUCATI — DUCATI PANIGALE V4 S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V031000·2025-01-23

    Honda and Acura fuel injection software error can stall the engine

    Honda is recalling certain 2022-2025 Acura MDX Type-S, 2023-2025 Pilot and 2021-2025 Acura TLX Type-S vehicles because a fuel injection control unit software error may cause an engine stall or loss of power.

    Product
    ACURA — ACURA, HONDA MDX TYPE S, TLX TYPE S, PILOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V033000·2025-01-23

    Subaru Forester alloy wheels may be improperly attached losing stability

    Subaru is recalling certain 2025 Forester vehicles with 18-inch aluminium alloy wheels because an incorrectly specified lug seat surface can leave the wheel improperly attached.

    Product
    SUBARU — SUBARU FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0887-2025·2025-01-22

    Life2000 Ventilation System battery charger defect causes device inoperability

    Baxter Healthcare is recalling the Life2000 Ventilation System due to a battery charger defect that can trigger an alarm, rendering the ventilator inoperable and unable to support patients' breathing.

    Product
    Breathe Technologies, Inc., Life2000 Ventilation System, REF BT-20-0002AP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0825-2025·2025-01-22

    ALTRUA 2 DR Pacemaker Models S702 and S722 Safety Mode Risk

    Boston Scientific ALTRUA 2 DR Pacemakers may unexpectedly enter Safety Mode during normal operation due to high battery impedance, potentially affecting device functionality.

    Product
    ALTRUA 2 DR Pacemaker, SL (Model Number S702) and EL (Model Number S722)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0884-2025·2025-01-22

    Welch Allyn Life 2000 Ventilator Battery Charger Defect Causes Inoperability

    The Welch Allyn Life 2000 Ventilator has a battery charger defect that could cause an alarm, rendering it inoperable. 187 units nationwide are affected in this FDA Class I recall.

    Product
    Welch Allyn, Inc., Life 2000 Ventilation System, REF BT-20-0002
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0425-2025·2025-01-22

    Wicklow Gold Cheddar Nettle & Chive Cheese recalled for possible Listeria contamination

    Abbey Specialty Foods is recalling Wicklow Gold Cheddar Nettle & Chive Cheese due to possible Listeria monocytogenes contamination. The product was distributed to Massachusetts, Colorado, and Ohio.

    Product
    Wicklow Gold Cheddar Nettle & Chive Cheese, 5.2 oz., plastic cryo-vac , 8 packages per case
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0395-2025·2025-01-22

    Cucumber Spears Recalled Due to Potential Salmonella Contamination

    First Quality Produce is recalling Cucumber Spears in 5-lb trays due to potential Salmonella contamination. The recall affects distribution to 13 consignees in California.

    Product
    Cucumber Spear; 5-lb plastic trays Brand: First Quality Produce
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-0830-2025·2025-01-22

    Impella RP Flex Devices Recalled Due to Optical Sensor Damage Risk

    Abiomed is recalling 2,364 units of the Impella RP Flex with SmartAssist due to risk of optical sensor damage from device interaction. Damage may cause temporary or permanent pump stop and loss of vital monitoring signals.

    Product
    Impella RP Flex with SmartAssist; Product Number: 1000323;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·003-2025·2025-01-22

    Custom Food Solutions Recalls Frozen Drunken Chicken for Undeclared Allergens

    Custom Food Solutions is recalling frozen drunken chicken due to undeclared egg and sesame allergens. No adverse reactions have been reported.

    Product
    Custom Food Solutions, LLC — Custom Food Solutions Recalls Ready-To-Eat Frozen Drunken Chicken Product Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0905-2025·2025-01-22

    Olympus MAJ-891 Forceps Recalled for Potential Biomaterial Retention During Reprocessing

    Olympus recalls the MAJ-891 endoscope forceps/irrigation plug nationwide because improper reprocessing may leave biomaterial inside the device, creating a contamination risk.

    Product
    Olympus MAJ-891 Forceps/Irrigation Plug (Isolated Type). Model/Catalog Number: MAJ-891. This instrument is designed to be attached to the instrument channel port of Olympus endoscopes to allow both irrigation and the use of endo-therapy accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0829-2025·2025-01-22

    Impella RP Heart Pump Recalled Due to Optical Sensor Damage Risk

    Abiomed is recalling 1,560 units of the Impella RP with SmartAssist pump due to risk of optical sensor damage from device interactions. Damaged sensors may cause temporary or permanent pump malfunction.

    Product
    Impella RP with SmartAssist; Product Number: 0046-0035;
    Category
    Medical Device
    Distribution
    Distributed nationwide