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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35526–35550 of 39777

  • SevereNHTSA·12V597000·2012-12-20

    Suzuki Recalls 2007 XL-7 Vehicles for Fuel Pump Module Cracking Risk

    American Suzuki is recalling 2,830 model year 2007 XL-7 vehicles in four states because a cracked fuel pump module could cause a fuel leak and potential fire.

    Product
    SUZUKI — SUZUKI XL7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V596000·2012-12-20

    Airstream Recalls 2008-2013 Interstates Due to Electrical Fire Risk

    Airstream is recalling 2008-2013 Interstate motorhomes with rear sofa floor plans because electrical equipment may contact metal components, posing a fire risk.

    Product
    AIRSTREAM — AIRSTREAM INTERSTATE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0818-2013·2012-12-19

    Lin-Mar Partners Recalls Longhorn Bars Due to Salmonella Risk

    Lin-Mar Partners Inc. is recalling Longhorn Bars because they may be contaminated with Salmonella, which can cause serious illness.

    Product
    Longhorn Bar Roasted Peanut with Chocolate (1.23 oz), 144 units per case. The bars are in packaging labeled as Longhorn Bars and have a picture of roasted peanuts and chocolate.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0812-2013·2012-12-19

    Berres Brothers Coffee Recalled for Undeclared Walnut Allergen

    Berres Brothers Coffee Roasters is recalling specific coffee products because they contain undeclared walnut, a major food allergen.

    Product
    Berres Brothers Coffee Roasters Mocha Monkey regular whole bean coffee packaged in 5 lb bulk bags with UPC 746774-00509.
    Category
    Food
    Distribution
    39 states
  • CriticalFDA (Food)·F-0816-2013·2012-12-19

    Berres Brothers Coffee Recalled for Undeclared Walnut Allergen

    Berres Brothers Coffee Roasters is recalling three coffee flavors because they contain undeclared walnut, a major food allergen.

    Product
    Berres Brothers Coffee Roasters Lunch with Elvis regular ground coffee packaged in the following sizes: 1.5 oz. (42.5g) with UPC 746774-000425, and 12 oz. (340g) bags with no UPC.
    Category
    Food
    Distribution
    39 states
  • CriticalFDA (Food)·F-0820-2013·2012-12-19

    Baugher's Unpasteurized Apple Cider Recalled Due to E. coli 0157:H7 Illnesses

    Baugher Enterprises is recalling unpasteurized apple cider linked to confirmed E. coli 0157:H7 foodborne illnesses. The product was sold in Maryland and the Gettysburg, PA area.

    Product
    Baugher's Apple Cider, one gallon and half gallon plastic jugs, with plastic caps labeled in part ***Fresh*** Preservatives added-keep under refrigeration***. Jugs are labeled in part ***FDA Required Warning: This product has not been pasteurized and therefore may contain…
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0819-2013·2012-12-19

    Lin-Mar Recalls Longhorn Peanut Butter Trail Mix Bars for Salmonella Risk

    Lin-Mar Partners Inc is recalling Longhorn Bar Peanut Butter Trail Mix Protein Bars due to potential Salmonella contamination.

    Product
    Longhorn Bar Peanut Butter Trail Mix (1.80 oz), 144 units per case. The bars are in packaging labeled as Longhorn Bars and have a picture of roasted peanuts and trail mix.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0814-2013·2012-12-19

    Berres Brothers Coffee Recalled for Undeclared Walnut Allergen

    Berres Brothers Coffee Roasters is recalling specific coffee products because they contain undeclared walnut, a major food allergen.

    Product
    Berres Brothers Coffee Roasters Lunch with Elvis regular whole bean coffee packaged in the following sizes: 12 oz. (340g) bags with no UPC, and 5 lb bulk bags with UPC 746774-5093
    Category
    Food
    Distribution
    39 states
  • SevereFDA (Food)·F-0817-2013·2012-12-19

    Berres Brothers Coffee Roasters Recalls Coffee for Undeclared Walnut

    Berres Brothers Coffee Roasters is recalling three coffee flavors because they contain undeclared walnut.

    Product
    Berres Brothers Coffee Roasters Lunch with Elvis decaffeinated ground coffee packaged in 12 oz. (340g) bags with no UPC.
    Category
    Food
    Distribution
    39 states
  • SevereFDA (Food)·F-0809-2013·2012-12-19

    Berres Brothers Coffee Recalled for Undeclared Walnut Allergen

    Berres Brothers is recalling specific coffee products because they contain undeclared walnut, a major food allergen.

    Product
    Berres Brothers Coffee Roasters Chocolate & Peanut Butter Decaffeinated whole bean coffee packaged in 12 oz. (340g) bags with no UPC code.
    Category
    Food
    Distribution
    39 states
  • SevereFDA (Food)·F-0811-2013·2012-12-19

    Berres Brothers Coffee Recalled for Undeclared Walnut Allergen

    Berres Brothers is recalling specific coffee products because they contain undeclared walnut, a major food allergen.

    Product
    Berres Brothers Coffee Roasters Chocolate & Peanut Butter Decaffeinated ground coffee packaged in 12 oz. (340g) bags with no UPC.
    Category
    Food
    Distribution
    39 states
  • SevereFDA (Food)·F-0810-2013·2012-12-19

    Berres Brothers Coffee Recalled for Undeclared Walnut Allergen

    Berres Brothers Coffee Roasters is recalling specific coffee products because they contain undeclared walnut, a major food allergen.

    Product
    Berres Brothers Coffee Roasters Chocolate & Peanut Butter regular ground coffee packaged in the following sizes: 1.5 oz. (42.5g) with UPC 746774-00042, 2.5 oz. with no UPC, and 12 oz. (340g) bags with UPC 746774-00359.
    Category
    Food
    Distribution
    39 states
  • SevereFDA (Devices)·Z-0497-2013·2012-12-19

    Medtronic SynchroMed II Pumps Recalled for Motor Stall Risk

    Medtronic is recalling SynchroMed II pumps because unapproved drugs can cause motor stalls and stop drug delivery.

    Product
    Medtronic SynchroMed II, Model 8637, (The SynchroMed¿ II Pump is supplied in 20 ml or 40 ml reservoir size.) Sterilized using ethylene oxide. The pump is part of an infusion system that stores and delivers a prescribed drug to a specific site. The implantable components of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0815-2013·2012-12-19

    Berres Brothers Coffee Recalled for Undeclared Walnut Allergen

    Berres Brothers Coffee Roasters is recalling specific coffee products because they contain undeclared walnut, a major food allergen.

    Product
    Berres Brothers Coffee Roasters Lunch with Elvis decaffeinated whole bean coffee packaged in 12 oz. (42.5g) bags with no UPC.
    Category
    Food
    Distribution
    39 states
  • SevereFDA (Devices)·Z-0478-2013·2012-12-19

    Verathon Recalls GlideScope Video Laryngoscopes Due to Blade Cracking

    Verathon is recalling GlideScope GVL3, GVL4, and GVL5 video laryngoscopes because their reusable blades may crack.

    Product
    The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that incorporates a high-resolution color camera, an LED light source, a rechargeable lithium battery, and video output to a remote monitor. It consists of a video laryngoscope and a portable video monitor. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0808-2013·2012-12-19

    Berres Brothers Coffee Recalled for Undeclared Walnut Allergen

    Berres Brothers Coffee Roasters is recalling specific coffee products because they contain undeclared walnut, a major food allergen.

    Product
    Berres Brothers Coffee Roasters Chocolate & Peanut Butter regular whole bean coffee packaged in the following sizes: 12 oz. (340g) UPC 746774-003594 and 5 LB bulk, UPC 746774-00499.
    Category
    Food
    Distribution
    39 states
  • SevereFDA (Food)·F-0813-2013·2012-12-19

    Berres Brothers Coffee Roasters Recalls Coffee for Undeclared Walnut

    Berres Brothers is recalling three coffee flavors because they contain undeclared walnut. Consumers should stop using the affected products.

    Product
    Berres Brothers Coffee Roasters Mocha Monkey regular ground coffee packaged in 1.5 oz. (42.5g) bags with UPC 746774-000425.
    Category
    Food
    Distribution
    39 states
  • SevereFDA (Food)·F-0807-2013·2012-12-19

    Turkana Valley Dried Apricots Recalled for Undeclared Sulfites

    Turkana Food Inc. is recalling Turkana Valley Dried Apricots because they contain undeclared sulfites, a potential allergen.

    Product
    Turkana Valley Dried Apricot 250 g, UPC 8692594007804 and 500 g UPC 8692594007811 Tunas Gida, San Ve Tic. Ltd. Sti 2 Org. San. Bol. Celal Dogan Bulvari No.:3 Baspinar Gaziantep/ Turkey packaged in plastic container
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0496-2013·2012-12-19

    Medtronic SynchroMed EL Pumps Recalled Due to Unapproved Drug Interactions

    Medtronic is recalling SynchroMed EL implantable infusion pumps because using unapproved drugs can cause the pump to stop working, halting drug delivery.

    Product
    SynchroMed EL, models 8626-10, 8626L-10, 8626-18, 8626L-18, 8627-10, 8627L-10, 8627-18, 8627L-18. implantable infusion pump. The pump is part of an implanted infusion system that consists of a SynchroMed EL pump and a catheter. The SynchroMed EL Infusion System is indicated…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V593000·2012-12-18

    Champion Bus Recalls Wheelchair Lifts Due to Fire Risk

    Champion Bus is recalling certain 2006-2013 buses because a wheelchair lift cable may cause a short circuit and fire.

    Product
    CHAMPION — CHAMPION, CHAMPION BUS CHALLENGER, DEFENDER, CRUSADER, AMERICAN CRUSADER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V588000·2012-12-17

    Autocar Recalls 2012-2013 Xpeditor Vehicles Due to Wheel Weld Defect

    Autocar is recalling 222 model year 2012-2013 Xpeditor vehicles because a weld defect may cause the wheel disc to separate from the rim, potentially leading to a crash.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·13071·2012-12-17

    Dunecraft Recalls Water-Absorbing Toys Due to Serious Ingestion Hazard

    Dunecraft is recalling Water Balz, Growing Skulls, H2O Orbs, and Fabulous Flowers toys because they can expand inside the body if swallowed, causing intestinal blockages.

    Product
    Water Balz, Growing Skulls, H2O Orbs "Despicable Me" and Fabulous Flowers toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V591000·2012-12-17

    New Flyer Transit Buses Recalled for Drive Shaft Access Panel Defect

    New Flyer is recalling 2,048 model year 2004-2011 transit buses because the drive shaft access panel may be insufficiently strong or secured, posing an injury risk if the drive shaft fails.

    Product
    NEW FLYER — NEW FLYER DE40LFR, DE40LFA, D40LFR, D60LF
    Category
    Vehicle
    Distribution
    Distributed nationwide