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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11626–11650 of 36636

  • SevereNHTSA·20V130000·2020-03-04

    Peterbilt Trucks Recalled for Battery Cable Fire Risk

    PACCAR is recalling 2015-2020 Peterbilt trucks because a battery cable may chafe and cause an electrical short circuit, increasing fire risk.

    Product
    PETERBILT — PETERBILT 579, 365, 389, 567
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1358-2020·2020-03-04

    Medline Robotic-LF Complete Delivery System Recall Due to Sterility Concerns

    Medline Industries is recalling 122 units of the Robotic-LF Complete Delivery System because the sterile packs did not complete a sterilization cycle, meaning sterility cannot be guaranteed.

    Product
    Medline ROBOTIC-LF REF CDS984543B Lot 20AKA927 Expiration 2020-09-30 GTIN (01)10888277056350
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1346-2020·2020-03-04

    Siemens COHERENCE Oncologist Software Recall for Incorrect Dose Positioning

    Siemens is recalling COHERENCE Oncologist software due to a calculation error that could lead to incorrect patient repositioning and radiation dose delivery to the wrong location.

    Product
    COHERENCE Oncologist, Model Nos. 07333680 & 07351898
    Category
    Medical Device
    Distribution
    16 states
  • SevereFDA (Food)·F-0737-2020·2020-03-04

    El Milagro Corn Tortillas Recalled for Potential Metal Inclusion

    El Milagro of Texas Inc. is recalling 2,400 packages of Original Corn/Maiz tortillas due to potential metal inclusion. The products were distributed in Texas.

    Product
    Original El Milagro Corn/Maiz tortillas 30 count Net Wt. 26 Oz. (750g) Refrigerate After Purchase UPC 649619621178
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·20V126000·2020-03-03

    Thomas Built Buses Recall 2019-2020 Models for Brake Caliper Bolt Issue

    Daimler Trucks is recalling 581 Thomas Built school buses because loose brake caliper bolts may reduce braking effectiveness, increasing crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX, SAF-T-LINER C2, SAF-T-LINER EFX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V125000·2020-03-03

    Blue Bird Recalls School Buses Due to Seat Barrier Defect

    Blue Bird is recalling 2008-2021 Vision and All American school buses because the seat barrier behind the driver may be missing a reinforcing bracket, increasing injury risk in a crash.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION SCHOOL BUS, VISION TRANSIT BUS, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V127000·2020-03-03

    Daimler Trucks Recalls 2019-2020 Vehicles for Brake Caliper Bolt Issue

    Daimler Trucks North America is recalling 2,585 2019-2020 trucks because brake caliper mounting bolts may be loose, increasing crash risk.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER, FCCC 4700, 5700, BUSINESS CLASS M2, XBR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V124000·2020-03-03

    Jeep Recalls Wrangler and Gladiator Vehicles for Clutch Fire Risk

    Chrysler is recalling 2018-2020 Jeep Wrangler and 2020 Gladiator vehicles with manual transmissions because the clutch pressure plate may overheat and fracture, increasing the risk of fire or crash.

    Product
    JEEP — JEEP WRANGLER, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V121000·2020-02-28

    Hyundai Recalls 2013-2014 Sonata Vehicles for Fuel Hose Fire Risk

    Hyundai is recalling 2013-2014 Sonata vehicles because a fuel hose may crack, causing a leak and increasing fire risk. Dealers will inspect and repair the hose free of charge.

    Product
    HYUNDAI — HYUNDAI SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V120000·2020-02-28

    Pierce Emergency Fire Vehicles Recalled for Aerial Device Cracks

    Pierce is recalling 2019-2020 Arrow XT, Enforcer, Impel, and Velocity fire vehicles because cracks in the aerial device tube may cause it to fall.

    Product
    PIERCE — PIERCE ARROW XT, IMPEL, VELOCITY, ENFORCER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20083·2020-02-27

    Lennox Recalls Ductless Heat Pumps Due to Fire Hazard

    Lennox is recalling about 1,650 ductless heat pumps sold in the U.S. because internal electrical components can fail and overheat, posing a fire hazard.

    Product
    Lennox Ductless Single-Zone and Multi-Zone heat pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V115000·2020-02-27

    Altec Recalls 2019 Aerial Devices Due to Fastener Failure Risk

    Altec Industries is recalling 238 specific 2019 aerial devices because high-strength fasteners securing the pedestal to the turntable may fail, potentially causing the pedestal to separate.

    Product
    ALTEC — ALTEC LR760-E70, TDA58, L42M, LR756
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V116000·2020-02-27

    GM Recalls 2020 Silverado and Sierra 1500 for Brake Caliper Bolt Defect

    General Motors is recalling 20,352 2020 Chevrolet Silverado 1500 and GMC Sierra 1500 vehicles because brake caliper bolts may break, increasing crash risk.

    Product
    GMC — GMC, CHEVROLET SIERRA 1500, SILVERADO 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1135-2020·2020-02-26

    Abbott NC TREK Coronary Dilatation Catheters Recalled for Balloon Deflation Issues

    Abbott Vascular is recalling NC TREK Coronary Dilatation Catheters because the balloon may be difficult or unable to deflate.

    Product
    NC TREK Coronary Dilatation Catheter, REF 1012454-20 Rx Only, NC TREK RX 4.50 X 20MM BDC The NC TREK RX Coronary Dilatation Catheter is indicated for: a) balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis, for the purpose of improving…
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-0942-2020·2020-02-26

    Philips Respironics Recalls Trilogy EVO Ventilators Due to Software Alarm Defect

    Philips Respironics is recalling 21 Trilogy EVO Ventilators because a software defect causes the loss of all power alarms.

    Product
    Trilogy EVO Ventilator, International, Model Number IN2110X15B Trilogy Evo is intended for pediatric through adult patients weighing at least 2.5 kg. The ventilator can measure, display, record, and alarm SpO2, FiO2, CO2, and Pulse Rate data when integrated with the…
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-0952-2020·2020-02-26

    Philips Respironics Recalls Trilogy EVO Ventilators Due to Software Defect

    Philips Respironics is recalling specific Trilogy EVO ventilators because a software defect causes power alarms to fail, potentially leaving patients without critical alerts.

    Product
    Trilogy EVO Ventilator, 02 - Iberia - Model Number: ES2100X15B Trilogy Evo is intended for pediatric through adult patients weighing at least 2.5 kg. The ventilator can measure, display, record, and alarm SpO2, FiO2, CO2, and Pulse Rate data when integrated with the…
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-0947-2020·2020-02-26

    Philips Respironics Recalls Trilogy EVO Ventilators Due to Software Alarm Defect

    Philips Respironics is recalling 15 Trilogy EVO Ventilators because a software defect causes the loss of all power alarms.

    Product
    Trilogy EVO Ventilator, Great Britain - Model Number: GB2110X15B Trilogy Evo is intended for pediatric through adult patients weighing at least 2.5 kg. The ventilator can measure, display, record, and alarm SpO2, FiO2, CO2, and Pulse Rate data when integrated with the…
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-0950-2020·2020-02-26

    Philips Respironics Recalls Trilogy EVO Ventilators Due to Software Defect

    Philips Respironics is recalling 21 Trilogy EVO Ventilators because a software defect causes the loss of all power alarms.

    Product
    Trilogy EVO Ventilator, 02 - International - Model Number: IN2100X15B Trilogy Evo is intended for pediatric through adult patients weighing at least 2.5 kg. The ventilator can measure, display, record, and alarm SpO2, FiO2, CO2, and Pulse Rate data when integrated with the…
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Food)·F-0711-2020·2020-02-26

    Hungry Root Dairy Free Garlic Parmesan Sauce Recalled for Undeclared Cashews

    The Honest Stand is recalling Hungry Root Dairy Free Garlic Parmesan Sauce because it contains cashews that were not listed on the physical packaging.

    Product
    Hungry Root Dairy free Garlic Parm sauce, Packaged in 9 oz. polypropylene dip containers with lidding film and lid, packed in 24 count master cases. Distributed by Hungry Root Inc. NY, NY 10003
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1136-2020·2020-02-26

    Abbott NC TREK Coronary Dilatation Catheters Recalled for Deflation Issues

    Abbott Vascular is recalling NC TREK Coronary Dilatation Catheters because the balloon may fail to deflate. The recall covers 39,687 units distributed worldwide.

    Product
    NC TREK Coronary Dilatation Catheter, REF 1012455-08 Rx Only, NC TREK RX 5.00 X 8MM BDC The NC TREK RX Coronary Dilatation Catheter is indicated for: a) balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis, for the purpose of improving…
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-1133-2020·2020-02-26

    Abbott NC TREK Coronary Dilatation Catheter Recall for Balloon Deflation Issues

    Abbott Vascular is recalling NC TREK Coronary Dilatation Catheters because the balloon may fail to deflate. The recall covers 39,687 units distributed worldwide.

    Product
    NC TREK Coronary Dilatation Catheter, REF 1012453-20 Rx Only, NC TREK RX 4.50 X 8MM BDC The NC TREK RX Coronary Dilatation Catheter is indicated for: a) balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis, for the purpose of improving…
    Category
    Medical Device
    Distribution
    0 states