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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13501–13525 of 89746

  • HighNHTSA·24V280000·2024-04-19

    2024 Coachmen Catalina and Forest River Aurora Travel Trailers Cooktop

    Forest River is recalling certain 2024 Coachmen Catalina and Forest River Aurora travel trailers because the cooktop-furnace isolation panel was not properly sealed during manufacturing, which could result in an inverted cooktop flame and fire risk.

    Product
    COACHMEN — COACHMEN, FOREST RIVER CATALINA, AURORA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24201·2024-04-18

    Gasaciods Children's Multi-Purpose Helmets Recalled for Head Injury Risk

    Gasaciods children's helmets sold on Temu.com fail to meet federal safety standards for bicycle helmets and do not adequately protect against head injury in a crash. Consumers should stop using them immediately.

    Product
    Gasaciods Children's Multi-Purpose Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V278000·2024-04-18

    2022 Jaguar E-Pace passenger air bag may tear during deployment

    Jaguar is recalling certain 2021–2023 E-Pace vehicles because the passenger air bag may tear during deployment, reducing occupant protection and risking burn injury from hot gases.

    Product
    JAGUAR — JAGUAR E-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24203·2024-04-18

    Gossamer Pro AGX+ Bicycle Cranksets Recalled for Fall Injury Risk

    Full Speed Ahead is recalling Gossamer Pro AGX+ cranksets that can loosen or detach from bicycles, creating a fall hazard. The company has received 277 reports of loosening or detachment but no injuries to date.

    Product
    Gossamer Pro AGX+ cranksets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V277000·2024-04-18

    Setra S407 and S417 Wheelchair Lift Beacon Recall

    Daimler Coaches is recalling 2011-2016 Setra coaches because wheelchair lift warning beacons may be too dim, increasing injury risk.

    Product
    SETRA — SETRA S407 CC, S417 TC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24202·2024-04-18

    Randder Liquid Fuel Bottles Recalled for Non-Child-Resistant Closure

    Randder 2-Pack Liquid Fuel Bottles in 750mL and 1500mL sizes sold on Amazon are recalled because their closures do not meet child-resistant requirements under the Children's Gasoline Burn Prevention Act, posing a risk of burns and poisoning to children.

    Product
    Randder 2-Pack Liquid Fuel Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1140-2024·2024-04-17

    Robeson Enterprises Mo' Money Pie Recalled for Undeclared Soy Allergen

    Robeson Enterprises is recalling Mo' Money Pie due to undeclared soy allergen on the label. The product was distributed to Georgia, North Carolina, and South Carolina.

    Product
    PIES & SIDES MO' MONEY PIE INGREDIENTS: BLACK EYED PEAS, COLLARDS, ELBOW PASTA, CHEESES, CORNMEAL, BLEACHED FLOUR, MILK PRODUCTS, SPICES. CONTAINS: MILK, EGG, WHEAT PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1147-2024·2024-04-17

    Dietary supplement recalled for toxic yellow oleander substitution

    Alipotec Raiz de Tejocote dietary supplements are being recalled because they contain toxic yellow oleander instead of tejocote. All 280 bottles were distributed nationwide.

    Product
    Alipotec Raiz de Tejocote dietary supplements, Net. Wt. 0.35oz, plastic bottle labeled with the "Alipotec King" sticker. Store at room temperature.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1484-2024·2024-04-17

    Ivenix Infusion System Software Recalled for Potential Dosing Anomalies

    Fresenius Kabi USA is recalling Ivenix Infusion System software version 5.8.0 for anomalies that could cause incorrect medication dosing or therapy delays. The Class I recall affects 17 units across 13 US states.

    Product
    LVP Software of the Ivenix Infusion System (IIS), Version 5.8.0.
    Category
    Medical Device
    Distribution
    13 states
  • SevereFDA (Food)·F-1139-2024·2024-04-17

    Baked Mac and Cheese Recalled for Undeclared Egg Allergen and Missing Ingredients

    Robeson Enterprises is recalling 482 units of PIES & SIDES Baked Mac and Cheese because the label fails to declare egg as an allergen and does not list any ingredients. Products were distributed to Georgia, North Carolina, and South Carolina.

    Product
    PIES & SIDES BAKED MAC AND CHEESE, ALLERGENS: MILK, PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1143-2024·2024-04-17

    Pumpkin Pie Recalled Due to Undeclared Milk and Egg Allergens

    Robeson Enterprises recalls PIES & SIDES brand pumpkin pie because the product label fails to list undeclared milk and eggs, posing a risk to consumers with these allergies.

    Product
    PIES & SIDES PUMPKIN PIE 10.5 oz INGREDIENTS: PUMPKIN FILLING, SUGARS, VANILLA, BLEACHED FLOUR, SPICES, CONTAINS: WHEAT PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0440-2024·2024-04-17

    FDA Class I Recall: Methocarbamol Injection for Particulate Matter

    Eugia US LLC is recalling Methocarbamol Injection nationwide due to particulate matter contamination. The FDA classified this as a Class I recall affecting lot 3MC23011 (expiration 11/30/2026).

    Product
    METHOCARBAMOL — METHOCARBAMOL (METHOCARBAMOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V273000·2024-04-17

    Spencer Recalls 2024 Pumper Vehicles Due to Electrical Fire Risk

    Spencer is recalling 2024 Pumper vehicles because a firmware defect in specific electrical nodes may cause overloaded circuits and increase the risk of fire.

    Product
    SPENCER — SPENCER PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1124-2024·2024-04-17

    Naturz Organics Pea Protein Recalled for Possible Salmonella Contamination

    Naturz Organics is recalling Organic Pea Protein (Item Code NO-OPP-80, 20 kg bags) due to possible salmonella contamination. The recall affects bulk product distributed to one consignee in Wisconsin.

    Product
    Naturz Organics Organic Pea Protein, Item Code NO-OPP-80, Net Weight 20 KG Bulk product packaged in paper bags.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1136-2024·2024-04-17

    Deep South Tomato Pie Recalled for Undeclared Eggs

    Robeson Enterprises is recalling Deep South Tomato Pie because the label does not list sub-ingredients, and pimento cheese in the product may contain undeclared eggs. Consumers with egg allergies should not consume this product.

    Product
    PIES & SIDES DEEP SOUTH TOMATO PIE, INGREDIENTS: SLICED TOMATOES, PIMENTO CHEESE, BLEACHED FOUR, MILK PRODUCTS, SPICES. CONTAINS: SOY, FISH, WHEAT, MILK PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • HighNHTSA·24V276000·2024-04-17

    2024 Tesla Cybertruck Accelerator Pedal Dislodgement Recall

    Tesla is recalling certain 2024 Cybertruck vehicles because the accelerator pedal pad may dislodge and become trapped by the interior trim, potentially causing unintended acceleration and crash risk.

    Product
    TESLA — TESLA CYBERTRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1510-2024·2024-04-17

    Hillrom Welch Allyn Spot Vision Screener recalled for power cord insulation defect

    Hillrom Welch Allyn Spot Vision Screener VS100 units recalled due to power cord insulation that does not meet electrical safety standards. The affected devices may pose an electrical hazard to users.

    Product
    Hillrom Welch Allyn Spot Vision Screener VS100, marketed under the following models: a) SPOT VISION SCREENER,W/O CASE,PLUG2/EUR, VS100-2; b) SPOT VISION SCREENER,W/O CASE,PLUG4/UK, VS100-4; c) SPOT VISION SCREENER,W/O CASE,PLUG7/SA, VS100-7; d) SPOT VISION…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1486-2024·2024-04-17

    Patient lift hanger bar may come loose, posing fall risks

    Certain patient lift models may have a hanger bar that could come loose during use, potentially causing patient falls. Approximately 10 units distributed to TX, IL, OK, and CA are affected.

    Product
    Altair 330 lbs w/o Hanger Bar, REF: 55200H-NA, 55220H-NA, and Roomer S 220 kg w/o Hanger Bar, REF: 55300H-NA, patient lifts
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1483-2024·2024-04-17

    KWIK-STIK Quality Control Kit Recalled for Fungal Contamination

    Microbiologics Inc recalls KWIK-STIK quality control kits contaminated with Aspergillus brasiliensis fungus. Users may observe unexpected fungal growth when using affected control material.

    Product
    KWIK-STIK Rhizopus stolonifer (+) derived from ATCC 6227b, a) REF 0209P and b) REF 0209K, Quality control kit for culture media
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1487-2024·2024-04-17

    Medline Adult Portable Bed Rails Recalled for Safety Standard Failures

    Medline is recalling certain lots of adult portable bed rails that were manufactured after the mandatory compliance date but failed to meet required safety standards, potentially posing a fall risk.

    Product
    Bed Assist Bars, labeled as follows: a) Medline, Model Number BA6800, b) Medline Martha Stewart, Model Number MDS6800BAMMS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1481-2024·2024-04-17

    Olympus Hemostasis Probe Mispackaged with Wrong Connector Type

    Olympus Corporation is recalling 36 units of Hemostasis Probe Model CD-B622LA that were mispackaged with the wrong connector type and labeled incorrectly. Healthcare facilities using the wrong device could experience use errors.

    Product
    Hemostasis Probe, Model: CD-B622LA
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1507-2024·2024-04-17

    CT Scanner Software Upgrade May Cause Unexpected Table Movement

    Philips CT scanner software upgrade may cause the patient tabletop to move unexpectedly during scan initialization, posing collision risk to nearby operators or bystanders.

    Product
    PHILIPS Incisive Computed tomography X-ray system Incisive CT Software Upgrade from V4.5.1.41921 to V4.5.1.41989-Intended to produce cross-sectional images of the body Model Number: 728143
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1129-2024·2024-04-17

    Whitley's Peanut Factory Deluxe Nut Mix recalled for undeclared allergens

    Whitley Peanut Factory is recalling Deluxe Nut Mix due to undeclared allergens (peanuts, milk, soy, wheat, and sesame) not listed on the product label. Consumers with allergies should not consume this product.

    Product
    Whitley's Peanut Factory, Deluxe Nut Mix, 12oz (340g), Electrolytic tin-plated cans, with paper label. 12-pack case boxes.
    Category
    Food
    Distribution
    28 states
  • HighFDA (Food)·F-1122-2024·2024-04-17

    Ground cinnamon bulk product recalled due to elevated lead levels

    Tasty-Sawa ground cinnamon in 55.11-pound bags distributed in Florida, Georgia, North Carolina, Trinidad and Tobago, and Guyana is being recalled due to elevated lead levels. Consumers should stop using this product immediately.

    Product
    Tasty-Sawa Cinnamon Ground, Net Wt. 55.11 lbs, paper bag (bulk), Country of Origin Vietnam
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1495-2024·2024-04-17

    ConvaTec CarboFlex Wound Dressing Recalled for Failed Sterility Standards

    ConvaTec is recalling 63 market units of CarboFlex odor control dressings that fail to meet sterility assurance requirements. Affected lots were distributed in six states.

    Product
    ConvaTec CarboFlex, 15cm x 20cm, 6 in. x 8 in., Order No. 403204, Odor Control Dressing, Sterile. Packaged 1 dressing/immediate package, 5 packages/market unit.
    Category
    Medical Device
    Distribution
    Distributed nationwide