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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3676–3700 of 36541

  • SevereFDA (Food)·F-1485-2024·2024-07-24

    Terrafina raw macadamia nuts recalled for salmonella contamination

    Terrafina macadamia nuts are being recalled because they tested positive for salmonella. The product was distributed in New Jersey and New York.

    Product
    Terrafina, Macadamia in the Raw , Net Wt. 6oz , (170 g)
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1493-2024·2024-07-24

    Aahu Barah Apricot Roll recalled for undeclared elevated sulfites

    Aahu Barah Apricot Roll (14 oz, UPC 882475000279) is being recalled because it contains elevated levels of undeclared sulfites. Consumers with sulfite sensitivity should not consume this product.

    Product
    Aahu Barah Apricot Roll; 14 oz; sold in clear plastic bags (6 inch x 8 inch) packing with the Aaha Barah label on the front and back; the product is labeled "Apricot Roll" on both the front and back; UPC 882475000279; label states "May Contain Sulfites As preservatives"
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-1476-2024·2024-07-24

    Multiple Spinach Products Recalled for Potential Listeria Contamination

    Multiple spinach products from various brands are being recalled due to potential Listeria monocytogenes contamination. The recall affects products distributed in New York, New Jersey, and New Hampshire.

    Product
    1. Greens Solata Spinach; 10x9 bag; UPC: 854311007391 / 2. Greens Full Circle Organic Baby Spinach; 6x10 Clamshell; UPC: 036800490512 / 3. Greens Solata Baby Spinach 6x10 clamshell; UPC: 85002149475 / 4. Greens Gaia Organic Baby Spinach 6x10 clamshell; UPC: 850021494837 / 5. Gre
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1481-2024·2024-07-24

    Spring Mix Herb Products Recalled for Potential Listeria monocytogenes Contamination

    Solata Food LLC is recalling three brands of spring mix herb products sold in NY, NJ, and NH due to potential contamination with Listeria monocytogenes, a bacterium that can cause serious illness.

    Product
    1. Greens Gaia Organic Spring Mix Herb; 8x45 clamshell; UPC: 850021494896 / 2. Greens Solata Spring Mix Herb; 8x5 clamshell; UPC: 854311007063 / 3. Greens Uncle Vinny's Spring Mix Herb; 8x5 clamshell; UPC: 804879459965
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·24V550000·2024-07-23

    Indian motorcycle rear suspension pushrods may buckle under load

    Indian Motorcycle is recalling certain 2024 Chieftain, Challenger, Pursuit, Roadmaster and Springfield motorcycles because the rear suspension pushrod may buckle under load.

    Product
    INDIAN — INDIAN ROADMASTER ELITE, SPRINGFIELD, ROADMASTER LIMITED, SPRINGFIELD DARK HORSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V545000·2024-07-23

    Capacity Recalls 2023 TJ Series Vehicles Due to Steering Gear Defect

    Capacity of Texas is recalling 2023 TJ 5000, 6500, and 9000 vehicles because steering gear assemblies may have fewer recirculating balls than required, risking loss of steering control.

    Product
    CAPACITY — CAPACITY TJ 5000, TJ 9000, TJ 6500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V546000·2024-07-22

    Motiv recalls electric chassis vehicles due to high-voltage software defect

    Motiv Power Systems is recalling 2019-2024 electric chassis vehicles because a software error may shut down high-voltage batteries, causing loss of power steering and braking.

    Product
    MOTIV — MOTIV E-450 BEV CHASSIS, F-59 BEV CHASSIS, F-53 BEV CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V543000·2024-07-19

    Blue Bird Recalls School Buses Due to Weak Roof Joints

    Blue Bird is recalling 2019-2023 Vision and All American school buses because roof joints may be too weak, risking panel separation in a crash.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS, ALL AMERICAN, ALL AMERICAN SCHOOL BUS, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V544000·2024-07-19

    Doosan Portable Generator Trailer Recalled for Improperly Tightened Lug Nuts

    Doosan is recalling 2024 Bobcat PG25 portable generator trailers because improperly tightened wheel lug nuts may allow wheels to detach, increasing crash risk.

    Product
    DOOSAN PORTABLE POWER — DOOSAN PORTABLE POWER MOBILE GENERATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V542000·2024-07-19

    Ford Recalls 2023-2024 Transit Vehicles for Steering Assist Loss Risk

    Ford is recalling 2023-2024 Transit vehicles with the Trail package because corrosion in the steering system may cause a loss of power assist, increasing crash risk.

    Product
    FORD — FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E061000·2024-07-19

    Ford Recalls Tie Rod Assemblies Due to Potential Steering Failure

    Ford is recalling specific front axle tie rod assemblies because incorrectly heat-treated ball studs may break, potentially causing loss of steering control.

    Product
    STEERING:LINKAGES:TIE ROD ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V538000·2024-07-18

    Chrysler Recalls 2019-2021 Pacifica Plug-In Hybrids for Fire Risk

    Chrysler is recalling 2019-2021 Pacifica Plug-In Hybrids because the battery pack may cause a vehicle fire while parked. Owners should park outside and avoid charging until repairs are completed.

    Product
    CHRYSLER — CHRYSLER PACIFICA PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V539000·2024-07-18

    Hyundai Recalls 2023 Xcient Trucks for Steering Control Risk

    Hyundai is recalling 2023 Xcient vehicles because the pitman arm may not be secured properly, which can result in a loss of steering control and increase the risk of a crash.

    Product
    HYUNDAI — HYUNDAI XCIENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V536000·2024-07-18

    Chrysler Recalls 2017-2018 Pacifica Plug-In Hybrids for Fire Risk

    Chrysler is recalling 2017-2018 Pacifica Plug-In Hybrid vehicles because the battery pack may cause a fire while parked. Owners should park outside and avoid charging until repairs are completed.

    Product
    CHRYSLER — CHRYSLER PACIFICA PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24307·2024-07-18

    CFMOTO ZFORCE 950 ROVs Recalled for Crash and Tip-Over Hazards

    CFMOTO is recalling approximately 3,630 ZFORCE 950 HO Sport Side-by-Side recreational off-highway vehicles from 2022–2023 because the shock absorber rod assembly can unthread and detach, causing suspension collapse and crash or tip-over hazards.

    Product
    CFMOTO ZFORCE 950 HO Sport Side-by-Side ROVs (2022-2023)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2252-2024·2024-07-17

    Medical Device Recall: Bausch+Lomb Intravitreal Injection Kit Unvalidated Sterilization

    Synergetics Inc is recalling Bausch+Lomb I-PACK Intravitreal Injection Kits because sterilization certificates could not be validated by the supplier. The FDA classified this as Class I.

    Product
    BAUSCH+LOMB, I-PACK Injection Kit with Drape, REF 18061, for the administration of intravitreal injection (eye)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1464-2024·2024-07-17

    Crecelac Infant Powdered Formula Recalled Due to Cronobacter

    Dairy Manufacturers' Crecelac Infant formula (5,376 cans distributed in Texas) is recalled due to Cronobacter spp. detected during FDA testing. Products lack required premarket evaluation for food safety and nutritional standards.

    Product
    Crecelac Infant 0-12 powdered infant formula with iron 12.4 oz cans
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1472-2024·2024-07-17

    Arepas La Mejor Arepa de Chocolo Recalled for Undeclared Milk Allergen

    Villa Nueva Interservices is recalling Arepas La Mejor Arepa de Chocolo due to undeclared milk allergen. Consumers with milk allergies are at risk.

    Product
    Arepas La Mejor, Arepa de Chocolo (Chocolate Sweet Corn Pancakes), NET WT. 25 Oz., 5 units per package, KEEP REFRIGERATED
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2253-2024·2024-07-17

    BAUSCH+LOMB I-PACK Injection Kit Recalled Due to Sterilization Validation Failure

    FDA has recalled 116 units of BAUSCH+LOMB I-PACK Injection Kits because sterilization certificates could not be validated by the supplier, creating potential infection risk for patients receiving intravitreal eye injections.

    Product
    BAUSCH+LOMB, I-PACK Injection Kit Custom, REF 18069, for the administration of intravitreal injection (eye)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2254-2024·2024-07-17

    Intravitreal Injection Kit Recalled for Unvalidated Sterilization Certificates

    Synergetics Inc is recalling 35 units of the BAUSCH+LOMB I-PACK Intravitreal Injection Kit because sterilization certificates could not be validated, creating an infection risk.

    Product
    BAUSCH+LOMB, I-PACK Injection Kit with Wire Speculum, REF 18069W, for the administration of intravitreal injection (eye)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2315-2024·2024-07-17

    Baxter iLED 7 surgical lights recalled due to thermal burn risk

    Baxter Healthcare is recalling iLED 7 surgical lights due to customer reports of thermal skin injuries. The recall affects approximately 6,243 units distributed worldwide.

    Product
    iLED 7 surgical lights, Model Numbers: a) 4068110 (Ceiling Single Surgical Light); b) 4068120 (Mobile Surgical Light); c) 4068140 (Pendant Surgical Light); d) 4068210 (Ceiling Duo Surgical Lights); e) 4068310 (Ceiling Trio Surgical Lights); f) 4068410 (Ceiling Quad
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-1463-2024·2024-07-17

    Powdered infant formula recalled for missing safety evaluation

    Farmalac powdered infant formula was recalled because the manufacturer failed to submit required premarket notification to the FDA. The product was never evaluated for safety or nutritional standards.

    Product
    Farmalac powdered infant formula with iron 12.4 oz cans
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1466-2024·2024-07-17

    Queso Rico La Hacienda Queso Fresco Cheese Recalled for Listeria

    Queso Rico La Hacienda brand queso fresco cheese was found to contain Listeria monocytogenes. FDA Class I recall affects 640 pounds distributed to retail stores in Texas counties.

    Product
    Queso Rico La Hacienda brand queso fresco cheese packaged in 9 oz, 1 pound, and 2 pound plastic packages. Product labeling reads in part "***QUESO RICO LA HACIENDA***EL QUESO FRESCO FRESCO DE VERACRUZ***Lic. Permit #483709 El Queso Rico "LA HACIENDA"***5617 E. Trenton Rd., Suite
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0588-2024·2024-07-17

    OTC Sunscreen Foundation Recalled for Fungal Mold Contamination

    Suntegrity IMPECCABLE SKIN sunscreen foundation is recalled for microbial contamination with Aspergillus Sydowii mold. Consumers should discontinue use immediately.

    Product
    IMPECCABLE SKIN - IVORY — IMPECCABLE SKIN - IVORY (ZINC OXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide