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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18501–18525 of 39605

  • CriticalUSDA FSIS·029-2018·2018-04-03

    Good Foods Recalls Curry Chicken Salad Due to Undeclared Cashews

    Good Foods Group is recalling ready-to-eat curry chicken salad cups because they contain undeclared cashews. The mislabeled products were distributed to retail locations in seven states.

    Product
    Good Foods Group, LLC — Good Foods Group, LLC Recalls Ready-To-Eat Chicken Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    7 states
  • SevereNHTSA·18V211000·2018-04-03

    Toyota Recalls 2017-2018 Models for Brake Booster Vacuum Pump Defect

    Toyota is recalling specific 2017-2018 Camry, Highlander, Sienna, Tacoma, and Lexus RX350 vehicles because a manufacturing defect in the brake booster vacuum pump may cause a sudden loss of brake assist.

    Product
    TOYOTA — TOYOTA, LEXUS TACOMA, SIENNA, RX350, HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·028-2018·2018-03-31

    PFP Enterprises Recalls Raw Beef Produced Without Federal Inspection

    PFP Enterprises is recalling approximately 7,146 pounds of raw beef products produced without federal inspection. Consumers are urged to discard or return the items.

    Product
    Patterson TMP Operating, LLC — PFP Enterprises LLC Recalls Raw Beef Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    9 states
  • SevereUSDA FSIS·027-2018·2018-03-29

    Target Recalls Frozen Meat and Poultry Due to Temperature Abuse

    Target is recalling frozen meat and poultry sold at a single Hawaii store due to temperature abuse during transport that may have allowed pathogen growth.

    Product
    Target Corporation Recalls Frozen Ready-To-Eat and Non-Ready-To-Eat Meat and Poultry Products due to Possible Temperature Abuse During Transport at a Single Store on Oahu, Honolulu, HI
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·18V208000·2018-03-29

    Mercedes-Benz Recalls 2018 Models for Driver Air Bag Inflator Defect

    Mercedes-Benz is recalling 2018 AMG GT, AMG GT C, GLC43 AMG, GLC300, and GLC350e vehicles because defective steel in the driver-side air bag inflator housing may cause rupture during deployment.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 350 E, GLC 300, AMG GLC43, AMG GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V203000·2018-03-29

    Alfa Romeo Stelvio Recall for Liftgate Wiring Water Leak

    FCA US LLC is recalling 2018 Alfa Romeo Stelvio vehicles because water leaks into liftgate wiring, causing corrosion that may allow the liftgate to open while driving.

    Product
    ALFA ROMEO — ALFA ROMEO STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V206000·2018-03-29

    Spartan Gladiator Recall for Front Axle Spindle Failure Risk

    Spartan Motors is recalling 2004-2007 Gladiator emergency response vehicles because front axle spindles may crack and fail, potentially causing a wheel to separate.

    Product
    SPARTAN — SPARTAN GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V199000·2018-03-29

    Navistar Recalls 2018-2019 International LT Trucks for Fuel Leak Risk

    Navistar is recalling 2018-2019 International LT trucks because a fender splash panel may rub against the fuel line, causing a leak that could lead to fire or crash.

    Product
    INTERNATIONAL — INTERNATIONAL LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E017000·2018-03-29

    Timoney Front Suspension Recall Due to Axle Spindle Fatigue Cracks

    Timoney Technology is recalling Mark 1 and Gen 2 Independent Front Suspensions because inconsistent machining may cause axle spindle failure and wheel separation.

    Product
    SUSPENSION:FRONT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V204000·2018-03-29

    Tesla Recalls Model S Vehicles Due to Steering Bolt Corrosion Risk

    Tesla is recalling 2012-2016 Model S vehicles because aluminum steering bolts may corrode and fracture, potentially causing a loss of power steering assist.

    Product
    TESLA — TESLA MODEL S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1526-2018·2018-03-28

    FDA Recalls Kratom Capsules Due to Potential Salmonella Contamination

    Pdx Aromatics is recalling specific lots of Kraken Kratom, Phytoextractum, and Soul Speciosa Green Vein Kratom capsules due to potential Salmonella contamination.

    Product
    GREEN Kratom CAPSULES, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The capsules are packaged in plastic heat sealed pouches. Each package sold in 28 grams (1 ounce), 56 grams (2 ounces), 112 grams (4 ounces). The varieties under each brand…
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1523-2018·2018-03-28

    Red Vein Kratom Powder Recalled for Potential Salmonella Contamination

    Pdx Aromatics is recalling Red Vein Kratom Powder products sold under Kraken Kratom, Phytoextractum, and Soul Speciosa brands due to potential Salmonella contamination.

    Product
    RED Vein Kratom POWDER, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The powder is packaged in plastic heat sealed pouches. Each package sold in 28 grams (1 ounce), 56 grams (2 ounces), and 112 grams (4 ounces). The varieties under each brand…
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1528-2018·2018-03-28

    Pdx Aromatics Recalls Kratom Capsules Due to Salmonella Contamination

    Pdx Aromatics is recalling specific lots of RED Vein Kratom Capsules sold under three brands due to potential Salmonella contamination.

    Product
    RED Kratom CAPSULES, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The capsules are packaged in plastic heat sealed pouches. Each package sold in 28 grams (1 ounce), 56 grams (2 ounces), 112 grams (4 ounces). The varieties under each brand…
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1525-2018·2018-03-28

    FDA Recalls Kratom Capsules Due to Potential Salmonella Contamination

    Pdx Aromatics is recalling White Vein Kratom capsules sold under three brands due to potential Salmonella contamination.

    Product
    WHITE VEIN Kratom CAPSULES, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The capsules are packaged in plastic heat sealed pouches. Each package sold in 28 grams (1 ounce), 56 grams (2 ounces), 112 grams (4 ounces). The varieties under each brand…
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1122-2018·2018-03-28

    MedComp Recalls 12F Tesio Catheter Sets Due to Connection Failure Risk

    Medical Components, Inc. is recalling 385 12F Tesio Catheter Sets because connection failures may cause blood loss or air emboli.

    Product
    12F Tesio CATHETER SET (CUFF 22CM FROM TIP), REF MCTC1235SD, UDI 884908027242 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0933-2018·2018-03-28

    Weis Markets Recalls Penne With Asiago Sauce And Grilled Chicken Meal

    Weis Markets is recalling Penne W/Asiago Sauce And Grilled Chix Small Meal due to undeclared milk. The product was sold in seven states.

    Product
    Weis Sunbury, PA 17801; Penne W/Asiago Sauce And Grilled Chix Small Meal; multiple weight. SCALE UPC - 205377-00000
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-1524-2018·2018-03-28

    Pdx Aromatics Recalls Kratom Powder Due to Salmonella Contamination Risk

    Pdx Aromatics is recalling specific lots of White Vein Kratom Powder sold under three brands due to potential Salmonella contamination.

    Product
    WHITE VEIN Kratom POWDER, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The powder is packaged in plastic heat sealed pouches. Each package sold in 28 grams (1 ounce), 56 grams (2 ounces), 112 grams (4 ounces), and 225 grams. The varieties under each…
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1127-2018·2018-03-28

    MedComp Repair Kit Recalled for Potential Connection Failures and Blood Loss Risk

    Medical Components, Inc. is recalling 1,575 MedComp Repair Kits due to potential connection failures that could lead to blood loss or air emboli.

    Product
    REPAIR KIT, REF RPK-01, UDI 884908039856 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1124-2018·2018-03-28

    MedComp Recalls 12F Tesio Catheter Sets Due to Connection Failure Risk

    Medical Components, Inc. is recalling 12F Tesio Catheter Sets because connection failures may cause blood loss or air emboli.

    Product
    12F Tesio CATHETER SET (CUFF 32CM FROM TIP), REF MCTC1247SD, UDI 884908027266 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1527-2018·2018-03-28

    Pdx Aromatics Recalls Kratom Powder Due to Salmonella Contamination

    Pdx Aromatics is recalling specific lots of Kraken Kratom, Phytoextractum, and Soul Speciosa GREEN VEIN Kratom POWDER due to potential Salmonella contamination.

    Product
    GREEN Kratom POWDER, sold under brand names Kraken Kratom, Phytoextractum, and Soul Speciosa. The powder are packaged in plastic heat sealed pouches. Each package sold in 28 grams (1 ounce), 56 grams (2 ounces), 112 grams (4 ounces). The varieties under each brand include…
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1118-2018·2018-03-28

    MedComp Recalls Catheter Repair Kits Due to Connection Failure Risk

    Medical Components, Inc. is recalling 93 Catheter Repair Kits because potential connection failures could lead to blood loss or air emboli.

    Product
    CATHETER REPAIR KIT, REF AAC52001, UDI 884908001891 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V201000·2018-03-28

    LGS Recalls 2018 Pace, Look, and Cargo Express Cargo Trailers

    LGS Industries is recalling 2018 Pace, Look, and Cargo Express cargo trailers because a spindle weld on the axle may fail, potentially causing loss of vehicle control.

    Product
    PACE — PACE, CARGO EXPRESS, LOOK CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1100-2018·2018-03-28

    Boston Scientific Recalls Malecot Nephrostomy Catheters Due to Breakage

    Boston Scientific is recalling Malecot Nephrostomy Catheter Sets because they may break at the mid-shaft bond during use.

    Product
    Malecot Nephrostomy Catheter Set, Product Number: M0064101000, GTIN: 08714729005261 The Malecot Nephrostomy Catheter Set is intended to establish percutaneous nephrostomy drainage and is indicated for the following: Diagnostic Indications: " Antegrade pyelography "…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1125-2018·2018-03-28

    MedComp Two Part Adapter Recall for Potential Connection Failures

    Medical Components, Inc. is recalling 35 MedComp Two Part Adapter kits due to potential connection failures that could cause blood loss or air emboli.

    Product
    TWO PART ADAPTER, REF MCTLA2000, UDI 884908027310 Product Usage: The Medcomp Repair Kit is indicated for use in replacing damaged female her connectors, clamps, or repairing extensions where there is a minimum of 4.5cm viable extension tubing.
    Category
    Medical Device
    Distribution
    Distributed nationwide