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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15601–15625 of 36701

  • SevereNHTSA·18V875000·2018-12-07

    Micro Bird Recalls CT-Series Buses for Seat Lock Defect

    Micro Bird is recalling 2015-2018 CT-Series buses because foldaway seats may not stay locked during a crash, increasing injury risk.

    Product
    MICRO BIRD — MICRO BIRD CT-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0678-2019·2018-12-05

    New Forest LLC Recalls Organic Cardamom Due to Salmonella Risk

    New Forest LLC is recalling 2,723 kgs of Organic Cardamom Green Whole from Guatemala due to potential Salmonella contamination. The product was distributed in Wisconsin and Nevada.

    Product
    Organic Cardamom Green Whole. Product of Guatemala. Product is labeled with a paper label son onto each 25-kg poly-lined, poly-weave "double bag". The label reads - Certified Organic Cardamom Pod Mixed Grade, Certified Organic by Mayacert, Product of Guatemala, Net Weight…
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-0664-2019·2018-12-05

    Imported Mexican Cheese Recalled Due to Salmonella Contamination

    Alebrije Imports Inc. is recalling Queseria "La Milagrosa" cheese due to Salmonella contamination found by the California Department of Food and Agriculture.

    Product
    Queseria "La Milagrosa" La Delicia al Paladar. 1/2 kg and 1 kg sizes. Packaged in a plastic bag with a yellow label.
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0722-2019·2018-12-05

    Chukar Cherries Ultra Dark Chocolate Cocoa Pecans Recalled for Unlabeled Milk

    Chukar Cherry Company is recalling 569 pouches of Ultra Dark Chocolate Cocoa Pecans because the product contains milk, which is not listed on the label.

    Product
    Ultra Dark Chocolate Cocoa Pecans, Chukar Cherries brand, packaged in 7.5 oz. plastic pouches. UPC 0 11261 22507 1. The label is read in parts: "***ULTRA DARK CHOCOLATE COCOA PECANS***Ingredients: Bittersweet Chocolate (Cacao Beans, Pure Cane Sugar, Unsweetened Chocolate…
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Devices)·Z-0507-2019·2018-12-05

    NxStage PureFlow B Solution Recalled for Potential Bag Bursting Hazard

    NxStage Medical is recalling PureFlow B Solution because the smaller chamber of the bag can burst, releasing electrolyte fluid that may cause injury if it contacts eyes or skin.

    Product
    NxStage PureFlow B Solution-RFP-RFP-456, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V864000·2018-12-05

    Volkswagen Recalls 2018 Golf R Vehicles Due to Fuel Hose Defect

    Volkswagen is recalling 2018 Golf R vehicles because a fuel hose connector may detach, causing a leak that increases fire risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN GOLF R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0514-2019·2018-12-05

    Eurotrol HemoTrol Level 2 Recalled Due to Microbial Contamination

    Eurotrol Inc. is recalling HemoTrol Level 2 hematology quality control mixtures because microbial contamination causes incorrect measurement results.

    Product
    HemoTrol Level 2- In Vitro Diagnostic Hematology quality control mixture Catalogue number: 171.002.002 Eurotrol HemoLin is an assayed hemoglobin control intended for professional use in the verification of the linearity of the HemoCue¿ Hb 201 systems
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0506-2019·2018-12-05

    NxStage PureFlow B Solution Recalled Due to Bag Bursting Risk

    NxStage Medical is recalling 7,275 units of PureFlow B Solution because the bag's smaller chamber may burst, releasing electrolyte fluid that can injure eyes or skin.

    Product
    NxStage PureFlow B Solution-RFP-RFP-454, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0470-2019·2018-12-05

    Synaptive Medical Recalls BrightMatter Guide Software Due to Defect

    Synaptive Medical Inc is recalling 37 units of BrightMatter Guide software due to a defect that occurs when switching between specific port trajectories during surgery.

    Product
    BrightMatter Guide, Product Number SYN-0026, Versions: 1.5.0, 1.5.1 and 1.5.2 Product Usage: BrightMatter Guide can navigate a third-party port (NICO BrainPath device) by attaching Synaptive s custom Tracking Array to the port directly. As the BrainPath is navigable in two…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V862000·2018-12-05

    Audi Recalls 2015-2016 A6 and A7 Models for Fire Risk

    Volkswagen is recalling 2015-2016 Audi A6 and 2015 A7 vehicles because an incorrectly inserted auxiliary heater connector may overheat and cause a fire.

    Product
    AUDI — AUDI A7, A6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0359-2019·2018-12-05

    Sandoz Losartan Potassium and Hydrochlorothiazide Tablets Recalled for NDEA Impurity

    Sandoz is recalling Losartan Potassium and Hydrochlorothiazide tablets because FDA testing found the impurity NDEA above acceptable levels.

    Product
    Sandoz Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 1000-count bottles, Rx Only, Finished Drug Product Manufactured by: Lek Pharmaceuticals d.d. SI-1526 Ljubljana,Sovenia for Sandoz Inc., Princeton, NJ 08540, NDC 0781-5207-10.
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0437-2019·2018-12-05

    Maquet Cardiovascular Recalls QUADROX-i Neonatal Membrane Oxygenators

    Maquet Cardiovascular is recalling QUADROX-i Neonatal membrane oxygenators due to a potential for blood leakage at the blood inlet connector when using a specific reducing screw adapter.

    Product
    QUADROX-i Neonatal with integrated arterial filter and VHK 11000 (VKMO 11000-USA#QUADROX-i Neo.+Reservoir), Part Number 701055207 The membrane oxygenator QUADROXi Neonatal is intended for use in extracorporeal circulation during cardiopulmonary bypass in cardiac surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0502-2019·2018-12-05

    NxStage PureFlow B Solution Recalled for Potential Bag Bursting and Injury

    NxStage Medical is recalling specific lots of PureFlow B Solution because the smaller chamber of the two-chamber bag can burst, releasing electrolyte fluid that may cause injury if it contacts eyes or skin.

    Product
    NxStage PureFlow B Solution-RFP-402, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0505-2019·2018-12-05

    NxStage PureFlow B Solution Recalled for Potential Bag Bursting

    NxStage Medical is recalling PureFlow B Solution because the bag's smaller chamber may burst, releasing electrolyte fluid that can injure eyes or skin.

    Product
    NxStage PureFlow B Solution-RFP-406, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V863000·2018-12-05

    Volkswagen Recalls 2018 Audi Models for Fuel Hose Fire Risk

    Volkswagen is recalling 2018 Audi A3 and TT models because a fuel hose connector may detach, causing a leak that increases fire risk.

    Product
    AUDI — AUDI A3 CABRIOLET, TT ROADSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V859000·2018-12-04

    Newmar Recalls 2018-2019 Motorhomes Due to Loose Brake Caliper Bolts

    Newmar is recalling 2018-2019 Essex, Ventana, and London Aire motorhomes because brake caliper mounting bolts may be loose, increasing crash risk.

    Product
    NEWMAR — NEWMAR VENTANA LE, VENTANA, ESSEX, LONDON AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·085-2018 EXP·2018-12-04

    JBS Tolleson Recalls Raw Beef Products Due to Salmonella Newport

    JBS Tolleson is recalling approximately 12.1 million pounds of raw beef products, including ground beef, due to possible Salmonella Newport contamination.

    Product
    JBS Tolleson Inc. — JBS Tolleson, Inc. Recalls Raw Beef Products due to Possible Salmonella Newport Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V857000·2018-12-03

    Gulf Stream Vintage Cruiser Recalled for Insufficient Bearing Grease

    Gulf Stream is recalling 2019 Vintage Cruiser recreational trailers because inner hub bearings may lack sufficient grease, risking overheating and hub failure.

    Product
    GULF STREAM — GULF STREAM VINTAGE CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V858000·2018-12-03

    McNeilus and Oshkosh Trucks Recalled for CNG Valve Defect

    McNeilus is recalling 2016-2018 trucks and Oshkosh S-Series vehicles because a CNG fuel tank valve stem may eject, posing injury and fire risks.

    Product
    MCNEILUS — MCNEILUS, OSHKOSH XE REAR LOADER, STANDARD MIXER, BRIDGEMASTER V MIXER, MERIDIAN FRONT LOADER 78
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E111000·2018-12-01

    Luxfer Recalls One-Turn Valves Due to Potential Stem Ejection Risk

    Luxfer Canada Ltd. is recalling One-Turn Valves (part number MPVE-250) because the valve stem may forcibly eject if the knob is turned more than one turn, posing injury and fire risks.

    Product
    FUEL SYSTEM, OTHER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide