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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11351–11375 of 36636

  • SevereNHTSA·20V234000·2020-04-27

    Blue Bird Recalls School Buses for Parking Brake Defect

    Blue Bird is recalling 2006-2021 Vision and 2007-2013 All American school buses because the parking brake may fail to hold the vehicle on an incline.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION, VISION TRANSIT BUS, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V235000·2020-04-27

    Blue Bird Recalls 2009-2019 Vision Buses for Parking Brake Defect

    Blue Bird is recalling 2009-2019 Vision transit buses because the floor-mounted parking brake may fail to hold the vehicle on an incline when fully loaded.

    Product
    BLUE BIRD — BLUE BIRD VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20112·2020-04-23

    Leviton Recalls 50-Ampere Electrical Connectors Due to Shock Hazard

    Leviton is recalling approximately 98,000 50-ampere electrical connectors, plugs, receptacles, and inlets sold in the US and Canada due to mislabeled terminal markings that pose an electrical shock hazard.

    Product
    Leviton 50 ampere, non-NEMA electrical connectors, plugs, receptacles and inlets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V231000·2020-04-23

    McLaren Recalls 2,763 Vehicles for Fuel Tank Corrosion Risk

    McLaren is recalling 2,763 vehicles because a foam pad may corrode the fuel tank, potentially causing a leak and fire risk.

    Product
    MCLAREN — MCLAREN 570 GT, SENNA, 720S, GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0892-2020·2020-04-22

    Mountain Rose Herbs Recalls Kudzu Root Due to Salmonella Risk

    Mountain Rose Herbs is recalling specific lots of Kudzu Root because they may be contaminated with Salmonella. The product was sold nationwide in the US and in Canada.

    Product
    Kudzu Root (Pueraria montana var. lobata), This product was packaged in a clear plastic bag or poly-woven bags sold in bulk form net weight ranges from 4 ounces to 20 pounds. The label is read in parts: "***Kudzu Root***Herbal Supplement **Origin: China** MOUNTAIN ROSE HERBS…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1717-2020·2020-04-22

    Sysmex CV-11 Sample Unit Recalled for Combustion Hazard

    Sysmex America is recalling 40 CV-11 Sample Units because urine spills on the transport track can reach electrical components, creating a potential for smoke, sparks, and combustion.

    Product
    Sysmex CV-11 Sample Unit, an integrated modular sampler that conveys specimens to either the UF-5000 or UD-10 analyzers.
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Drugs)·D-1238-2020·2020-04-22

    Losartan Potassium Tablets Recalled Due to NBMA Impurity Detection

    Golden State Medical Supply Inc. is recalling Losartan Potassium Tablets 25 mg because an impurity, NBMA, was detected in the active ingredient.

    Product
    Losartan Potassium Tablets, USP, 25 mg, Rx only, a) 30 ct. (NDC 60429-316-30) b) 90ct. (NDC 60429-316-90) c) 1,000 ct. (60429-316-10) bottles, GSMS Incorporated, Manufactured by Arrow Pharm (Malta) Ltd., Packaged by GSMS Incorporated, Camarillo, CA 93012, USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1214-2020·2020-04-22

    Bi-Est Cream Recalled for Lack of Processing Control

    The Medicine Shoppe Pharmacy is recalling Bi-Est cream due to lack of processing control. The product was distributed in Florida.

    Product
    Bi-Est (50/50)/Progesterone/Testost 1.5/100/0.5 mg Cream 30 gm tube, Rx, The Medicine Shoppe Pharmacy, Port Charlotte, FL
    Category
    Drug
    Distribution
    1 state
  • SevereNHTSA·20V230000·2020-04-22

    Lode King Prestige Semi-Trailers Recalled for Cargo Winch Mount Defect

    Lode-King is recalling 2015-2021 Prestige SDG53-2 step-deck semi-trailers because cargo winch mounts may fail, allowing cargo to fall off and create road hazards.

    Product
    LODE KING — LODE KING PRESTIGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1700-2020·2020-04-22

    Abbott Recalls Merlin PCS 3650 Software Upgrade Kit Due to Anomaly

    Abbott is recalling the Merlin PCS 3650 Software Upgrade Kit because a software anomaly may cause the device to use a previously programmed shock energy level without alerting the user.

    Product
    Merlin PCS 3650 Software Upgrade Kit, REF 3330 St. Jude Medical The MerlinTM Patient Care System (MerlinTM PCS) Model 3650 is a portable, dedicated programming system designed to interrogate, program, display data, and test St. Jude MedicalTM implantable devices and leads.
    Category
    Medical Device
    Distribution
    40 states
  • SevereNHTSA·20V225000·2020-04-21

    Altec Recalls 2017-2020 ST Spray Trucks Due to Electrical Fire Risk

    Altec is recalling 92 ST Spray Trucks from 2017-2020 because an improperly mounted battery fuse holder may cause an electrical short circuit and fire.

    Product
    ALTEC — ALTEC ST SPRAY TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V223000·2020-04-20

    Eldorado CNG Vehicles Recalled for Fuel System Rupture Risk

    Eldorado is recalling 2018-2020 CNG-powered vehicles because the pressure relief device may fail to vent heat, potentially causing the fuel system to rupture.

    Product
    ELDORADO — ELDORADO XHF, E-Z RIDER II, AXESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V222000·2020-04-20

    TransitWorks Recalls Driverge Vans for Seat Belt Retract Issues

    TransitWorks is recalling 2019-2020 Ford Transit and RAM ProMaster vans because seat belt retractors may not secure occupants properly.

    Product
    RAM — RAM, FORD PROMASTER, TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V219000·2020-04-17

    International DuraStar and WorkStar Fuel Heater Fire and Engine Stall Recall

    Navistar is recalling 2017-2020 International DuraStar and WorkStar models, plus IC bus vehicles with Cummins B6.7 engines. The electric fuel heater may overheat and catch fire or cause engine stalling.

    Product
    IC BUS — IC BUS, INTERNATIONAL TC, CE, MV, DURASTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20733·2020-04-16

    Polaris Recalls 2018-2020 Ranger XP 1000 Off-Road Vehicles Due to Fire Hazard

    Polaris is recalling approximately 80,000 Model Year 2018-2020 Ranger XP 1000 and CREW XP 1000 off-road vehicles because a broken clutch belt can damage the fuel line and cause a fire.

    Product
    Model Year 2018 - 2020 Ranger XP 1000 & CREW XP 1000 Off-Road Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0891-2020·2020-04-15

    Koi Koi Trading Recalls Fresh Salmon Due to Listeria Risk

    Koi Koi Trading is recalling fresh salmon in Southern California because the product may be contaminated with Listeria monocytogenes.

    Product
    Fresh Salmon; Brand names : Bakka, Superior, Scottish Canada, Ocean Quality, Norway. Refrigerate Unit size: 10-12 lbs., 14-16 lbs., 16-18 lbs., 18-20 lbs,; packed in Styrofoam box; 2 pieces, 3 pieces or 4 pieces in the box.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1103-2020·2020-04-15

    Avet Pharmaceuticals Recalls Losartan Potassium Tablets Due to Impurity

    Avet Pharmaceuticals is recalling Losartan Potassium Tablets 50 mg because FDA testing found an impurity above acceptable levels.

    Product
    Losartan Potassium Tablets USP 50 mg, a) 30 count (NDC 23155-645-03), b) 90 count (NDC 23155-645-09) and c) 1000 count (NDC 23155-645-10) bottles, Rx only, Manufactured by: Vivimed Life Sciences Private Limited, Tamil Nadu, India, Manufactured for: Heritage Pharmaceutical Inc.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1679-2020·2020-04-15

    Siemens ONCOR Radiation Therapy Systems Recalled for Potential Dose Overdose

    Siemens is recalling specific ONCOR radiation therapy systems due to a potential safety issue with dose monitoring interlocks that could result in a 10-20% overdose.

    Product
    ONCOR Avante Garde #5863472, ONCOR Expression #7360717, ONCOR Impression #5857920, ONCOR Impression Plus #5857912 with Digital LINAC Systems Control Console Software Versions 6, 7, 9, 13
    Category
    Medical Device
    Distribution
    35 states