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.

Filters

Agency

Category

Minimum severity

Clear filters

35576–35600 of 39777

  • SevereNHTSA·12V576000·2012-12-11

    Daimler Recalls 2007 Sterling 360 Trucks for Fuel Line Fire Risk

    Daimler Trucks North America is recalling 2007 Sterling 360 trucks because fuel lines may crack or flare nuts may be loose, creating a fire hazard.

    Product
    STERLING — STERLING 360
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V573000·2012-12-11

    Honda Recalls 2003-2006 Vehicles for Ignition Switch Interlock Defect

    Honda is recalling specific 2003-2006 Pilot, Odyssey, and Acura MDX vehicles because a deformed ignition switch lever may allow the vehicle to roll away if the key is removed without shifting to park.

    Product
    HONDA — HONDA, ACURA ODYSSEY, MDX, PILOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V574000·2012-12-11

    Thor Motor Coach Recalls 727 RVs for Cruise Control Defect

    Thor Motor Coach is recalling 727 recreational vehicles because loose diode jumpers may prevent cruise control from disengaging or brake lights from illuminating.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TUSCANY, ULTRASPORT, MONTECITO, PALAZZO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V577000·2012-12-10

    Champion Transit Buses Recalled for Cruise Control and Brake Light Defect

    Champion Bus is recalling 49 transit buses from 2011-2013 because loose connectors may prevent cruise control from disengaging or brake lights from illuminating.

    Product
    CHAMPION — CHAMPION CX380, CX300, 3035RE, CX340
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V580000·2012-12-10

    Glaval Transit Buses Recalled for Wheelchair Lift Cable Fire Risk

    Glaval is recalling 2007-2012 transit buses because a wheelchair lift cable may cause a short circuit and fire.

    Product
    GLAVAL — GLAVAL, GLAVAL BUS SPORT, TITAN, TITAN II, UNIVERSAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V571000·2012-12-07

    Jaguar Recalls 2013 XF Vehicles Due to Fuel Pump Shutdown Risk

    Jaguar is recalling 2013 XF vehicles because electronic modules may shut down the fuel pump, causing the engine to stall and increasing crash risk.

    Product
    JAGUAR — JAGUAR XF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V569000·2012-12-07

    Coach and Equipment Recalls Phoenix and Metro-Lite Transit Buses

    Coach and Equipment is recalling 2006-2012 Phoenix and 2007/2009 Metro-Lite transit buses because a wheelchair lift cable may cause a short circuit and fire.

    Product
    COACH & EQUIPMENT — COACH & EQUIPMENT PHOENIX, METRO-LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V566000·2012-12-06

    Winnebago and Itasca Motorhomes Recalled for Electrical Connector Defect

    Winnebago is recalling 2010-2013 Itasca and Winnebago motorhomes because loose electrical connectors may prevent brake lights from working or cruise control from disengaging.

    Product
    ITASCA — ITASCA, WINNEBAGO MERIDIAN, ELLIPSE, TOUR, JOURNEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·13061·2012-12-06

    Dream On Me Recalls Baby Bath Seats Due to Drowning Hazard

    Dream On Me is recalling approximately 50,000 baby bath seats because they can tip over, posing a drowning risk to infants.

    Product
    Dream On Me Bath Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V563000·2012-12-06

    Land Rover Recalls 2012 LR2 and Evoque for Brake Caliper Bolts

    Jaguar Land Rover is recalling 2012 LR2 and Range Rover Evoque vehicles because rear brake caliper bolts may be insufficiently torqued, posing a crash risk.

    Product
    LAND ROVER — LAND ROVER LR2, RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0161-2013·2012-12-05

    Medpro Elastomeric Infusion Pump Recalled for Higher Flow Rate

    First Medical Source LLC is recalling 500 units of Medpro Elastomeric Infusion Pumps because they may deliver medication at a higher flow rate than specified, risking over-administration.

    Product
    Medpro Elastomeric Infusion Pump. AccuFlux, Model # CT-0020-100H. Product Usage: The devices are intended for patients requiring intravenous, percutaneous, subcutaneous, intra-operative sites or epidural administration of medications. It is the responsibility of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0735-2013·2012-12-05

    Kroger Ice Cream Recalled for Potential Pecan Allergen Contamination

    Kroger is recalling French Vanilla Magnifique Ice Cream because it may contain pecans, posing a severe allergic reaction risk to sensitive individuals.

    Product
    Kroger Deluxe French Vanilla Magnifique Ice Cream, 48 FL OZ laminated carton. INGREDIENTS: MILK, CREAM, SUGAR***CONTAINS: MILK, EGGS DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202***800-632-6900 or www.kroger.com.
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·F-0737-2013·2012-12-05

    Nestle Recalls Nesquik Chocolate Powder Due to Salmonella Risk

    Nestle is recalling specific lots of Nesquik Chocolate Powder because ingredients may be contaminated with Salmonella.

    Product
    Nesquik Chocolate Powder, 1) 6x40.7oz, UPC 0 28000 68230 9. 2) 12x21.8oz, UPC 0 28000 68090 9. 3) 12x10.9oz, UPC 0 28000 67990 3.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0740-2013·2012-12-05

    United Dairy Farms Ice Cream Recalled for Potential Salmonella Contamination

    United Dairy Farmers Inc is recalling Oatmeal Cookie Overload Ice Cream because it may contain salmonella. The product was distributed in Ohio, Indiana, Kentucky, and Michigan.

    Product
    United Dairy Farms brand Oatmeal Cookie Overload Ice Cream 3 gallon, corrugated square
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-068-2013·2012-12-05

    GlaxoSmithKline Recalls Arranon Injection Due to Potential Impurities

    GlaxoSmithKline is recalling specific lots of Arranon (nelarabine) Injection because drug-related impurities may exceed specification limits.

    Product
    Arranon (nelarabine) Injection 5mg/mL, 50mL Vials, Rx only, For I.V. Infusion only, GlaxoSmith Kline, Research Triangle Park, NC 27709. Made in England, NDC 0007-4401-06
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0726-2013·2012-12-05

    BumbleBar Recalls Gluten Free Cafe Chocolate Sesame Bars Due to Salmonella Risk

    BumbleBar, Inc. is recalling Gluten Free Cafe Chocolate Sesame Bars because they contain roasted peanuts from Sunland Inc. that may be contaminated with Salmonella.

    Product
    Gluten Free Cafe Chocolate Sesame Bar. The Retail Carton has a UPC 70795-03450 and the Individual Bar has a UPC 70795-03550. The product is labeled in parts: "***Chocolate Sesame Bars With Flax Seeds & Roasted Peanuts***gluten free cafe***NET WT .95 OZ (27g)…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0732-2013·2012-12-05

    Bolthouse Farms Carrot Chips Recalled Due to Salmonella Contamination

    Bolthouse Farms is recalling Carrot Chips after random sampling by the North Carolina Department of Agriculture found Salmonella. The product was distributed in the US and Canada.

    Product
    Bolthouse Farms Carrot Chips (Croustilles Aux Carottes). No Preservatives. Product of the U.S.A. Net Wt. 16 oz (1 lb) 454 b poids net. UPC 71464 17209 Product was also packed under brand names of Safeway Farms, UPC 21130 70217 and Farm Stand (private label for…
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0731-2013·2012-12-05

    Murray's Waffle Cone Dip Recalled for Undeclared Milk and Soybean Oil

    CSM Bakery Products NA is recalling Murray's Waffle Cone Dip due to undeclared milk and soybean oil allergens caused by mislabeling.

    Product
    Murray's WAFFLE CONE DIP, NET WEIGHT - 7 lb 8 oz (3.40 kg), Product Item Code 835462, Bar code 0 06847 66003 2. The product is packaged in # 10 cans, 3 cans per case.
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0725-2013·2012-12-05

    BumbleBar Gluten Free Cafe Cinnamon Sesame Bar Recalled for Salmonella Risk

    BumbleBar, Inc. is recalling Gluten Free Cafe Cinnamon Sesame Bars due to potential Salmonella contamination from roasted peanuts.

    Product
    Gluten Free Cafe Cinnamon Sesame Bar. The Retail Carton has a UPC 70795-03451 and the Individual Bar has a UPC 70795-03551. The product is labeled in parts: "***Cinnamon Sesame Bars With Flax Seeds & Roasted Peanuts***gluten free cafe***NET WT .95 OZ (27g)…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-063-2013·2012-12-05

    Samantha Lynn Recalls Reumofan Plus Tablets for Undeclared Ingredients

    Samantha Lynn, Inc. is recalling Reumofan Plus Tablets because they contain undeclared drug ingredients, making them unapproved drugs.

    Product
    Reumofan Plus Tablets, 30-count bottle per Box, (remaining label information in Spanish)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0435-2013·2012-12-05

    Terumo Advanced Perfusion System 1 Recalled for Total Loss of Functionality

    Terumo is recalling 1,647 Advanced Perfusion System 1 units because they may shut down completely, stopping pumps and failing to activate battery backup.

    Product
    100/120V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion System 1 is indicated for use for up to 6 hours on the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when used by a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0436-2013·2012-12-05

    Terumo Advanced Perfusion System 1 Recalled for Power Loss

    Terumo is recalling Advanced Perfusion System 1 units that may lose power and shut down during use, causing pumps to stop.

    Product
    220/240V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion System 1 is indicated for use for up to 6 hours on the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when used by a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-070-2013·2012-12-05

    Ranbaxy Recalls Atorvastatin Calcium Tablets Due to Glass Particulates

    Ranbaxy Inc. is recalling certain lots of Atorvastatin Calcium tablets because they may contain small glass particulates.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide