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 deaths or serious injuries are reported, 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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10326–10350 of 36631

  • SevereNHTSA·20V770000·2020-12-10

    Honda and Acura Recall Vehicles for Potential Drive Shaft Breakage

    Honda is recalling specific 2007-2015 Acura and Honda models because improperly coated drive shafts may break, causing loss of power or vehicle roll-away.

    Product
    ACURA — ACURA, HONDA ILX, CIVIC HYBRID, FIT, ILX HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V767000·2020-12-10

    2020-2021 Forest River XLR Toy Hauler Weight Label Defect Recall

    Forest River is recalling certain 2020-2021 XLR Boost Toy Hauler recreational vehicles with inaccurate Federal Placards that may understate the vehicle's weight, risking tire damage and crashes from overloading.

    Product
    FOREST RIVER — FOREST RIVER XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V765000·2020-12-10

    Altec Recalls 2018-2020 Digger Derricks Due to Hydraulic Valve Defect

    Altec is recalling 2018-2020 digger derricks and aerial devices because a hydraulic check valve snap ring can fail, causing unintended boom movement.

    Product
    ALTEC — ALTEC DIGGER DERRICK, AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0118-2021·2020-12-09

    MPM Medical Recalls REGENECARE HA Topical Anesthetic Due to Bacteria

    MPM Medical LLC is recalling REGENECARE HA topical anesthetic hydrogel because it was found to be contaminated with Burkholderia cepacia bacteria.

    Product
    REGENECARE HA — REGENECARE HA (LIDOCAINE HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0144-2021·2020-12-09

    Dole Organic Romaine Hearts Recalled Due to E. coli Contamination

    Dole Fresh Vegetables Inc. is recalling specific lots of Organic Romaine Hearts because pathogenic non-O157 E. coli STEC was found during routine sampling.

    Product
    Dole" Organic Romaine Hearts 3pk Organic Biologique) (UPC 0-71430-90061-1), Wild Harvest Organic Romaine Hearts, Net Wt 12 oz. (UPC 7-11535-50201-2),
    Category
    Food
    Distribution
    14 states
  • CriticalFDA (Drugs)·D-0111-2021·2020-12-09

    Lohxa Recalls Chlorhexidine Gluconate Oral Rinse Due to Bacterial Contamination

    Lohxa LLC is recalling Chlorhexidine Gluconate Oral Rinse USP, 0.12%, due to contamination with Burkholderia lata bacteria.

    Product
    Chlorhexidine Gluconate Oral Rinse USP, 0.12%, Alcohol Free, packaged in 15 mL unit does cups (barcode 7016602715), packaged in 50-count unit dose cups per carton, Rx only, Distributed by: Lohxa, Worcester, MA 01608, NDC 70166-027-15
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0527-2021·2020-12-09

    CME America T-Syringe Pump Recall for Motor Wear and Fluid Damage

    CME America is recalling T34L PCA syringe pumps because motor wear may cause under-infusion without alarms, and cleaning fluids may damage hardware.

    Product
    CME America T-Syringe Pump - T34L PCA - Product Usage: infusion of medications or fluids requiring continuous or intermittent delivery at precisely-controlled infusion rates through clinically acceptable routes of administration, including intravenous, subcutaneous, percutaneous,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0514-2021·2020-12-09

    Invacare PerfectO2 V Oxygen Concentrator Recalled for Fire and Explosion Risk

    Invacare is recalling 384,767 PerfectO2 V oxygen concentrators worldwide due to a defect that may cause self-extinguishing fires or cap explosions.

    Product
    Invacare PerfectO2 V Oxygen Concentrator- intended for patients with respiratory disorders requiring supplemental oxygen Model Numbers: IRC5PO2V (US), IRC5PO2VC (Canada), All World: IRC5PO2VAW, IRC5PO2VAWL2, IRC5PO2VAWL3, IRC5PO2VAWL4, IRC5PO2VAWL5
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·21046·2020-12-09

    L G Sourcing Recalls Electric Fireplaces Due to Fire Hazard

    L G Sourcing is recalling allen + roth 62-inch electric fireplaces sold at Lowe's because wiring connectors can overheat, posing a fire hazard.

    Product
    allen + roth 62-inch Electric Fireplaces
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0145-2021·2020-12-09

    Tanimura & Antle Romaine Lettuce Recalled Due to E. coli O157:H7 Detection

    Tanimura & Antle is recalling specific lots of Romaine lettuce after Michigan state officials detected E. coli O157:H7 during routine sampling.

    Product
    Tanimura & Antle brand Romaine lettuce. 1 head 12,15,018 and 24 case Product of USA UPC: 2-27918 20314-9 Tanimura & Antle, Salinas, CA
    Category
    Food
    Distribution
    19 states
  • SevereNHTSA·20V760000·2020-12-09

    Audi Recalls 2018-2019 RS 5 Coupe for Battery Terminal Cover Defect

    Audi is recalling 2,355 2018-2019 RS 5 Coupe vehicles because an incorrect positive battery terminal cover could prevent doors from opening or hazard lights from working after a rear crash.

    Product
    AUDI — AUDI RS 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0516-2021·2020-12-09

    Medtronic MiniMed 670G Insulin Pumps Recalled for Battery Connection Defect

    Medtronic is recalling 391 MiniMed 670G insulin pumps because a missing solder battery connection could interrupt power to the device.

    Product
    MiniMed 670G, insulin pump, Ref/Model # MMT-1760KPK, MMT-1762KCN, MMT-1762WWK - Product Usage: indicated for continuous or periodic monitoring of glucose levels in the fluid under the skin, and detecting possible low and high glucose episodes. When using a sensor and transmitter,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0526-2021·2020-12-09

    CME America Recalls NeoThrive Syringe Pumps Due to Motor Wear

    CME America is recalling 4,182 NeoThrive syringe pumps because motor wear may cause under-infusion without alarms, and cleaning fluids may damage hardware.

    Product
    CME America T-Syringe Pump - NeoThrive - Product Usage: infusion of medications or fluids requiring continuous or intermittent delivery at precisely-controlled infusion rates through clinically acceptable routes of administration, including intravenous, subcutaneous, percutaneous
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0518-2021·2020-12-09

    Medtronic MiniMed 640G Insulin Pump Recalled for Missing Solder Battery Connection

    Medtronic is recalling MiniMed 640G insulin pumps because a missing solder battery connection could interrupt power. The recall covers specific serial numbers distributed in the U.S. and abroad.

    Product
    MiniMed 640G, insulin pump, Ref/Model # MMT-1711K, MMT-1752K, MMT-1752, Rx Only - Product Usage: indicated for the continuous delivery of insulin, at set and variable rates, for the management of diabetes mellitus in persons requiring insulin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V759000·2020-12-08

    Nissan Recalls 2020 Titan Trucks Due to Engine Wiring Fire Risk

    Nissan is recalling 2020 Titan and Titan XD trucks because an exposed wire in the engine harness could cause an electrical short, leading to engine stall or fire.

    Product
    NISSAN — NISSAN TITAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V755000·2020-12-07

    Infiniti Recalls M56, Q70, and Hybrid Models for Driveshaft Defect

    Nissan is recalling specific Infiniti models because a broken driveshaft can cause loss of propulsion or disable the parking brake, increasing crash risk.

    Product
    INFINITI — INFINITI M56, Q70, M35 HYBRID, Q70 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0132-2021·2020-12-02

    Whole Foods Recalls Fried Chicken Meals for Potential Undeclared Egg

    Whole Foods Market is recalling Fried Chicken Meals with Mac & Cheese in five states and D.C. due to a potential undeclared egg allergen.

    Product
    Fried Chicken Meal with Mac & Cheese, packaged in clear plastic container with printed label product code begins with 247257; Fried Chicken Meal with Mac & Cheese, packaged on hot bar product code begins with 237444
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0135-2021·2020-12-02

    Whole Foods Recalls BBQ Turkey Meatballs for Undeclared Egg

    Whole Foods Market is recalling BBQ Turkey Meatballs Chef Plates due to a potential undeclared egg allergen. The product was distributed in Maryland, New Jersey, Pennsylvania, Virginia, and Washington, D.C.

    Product
    BBQ Turkey Meatballs Chef Plate with Mac & Cheese and Green Beans, packaged in clear plastic container with printed label product code begins with 241464
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0131-2021·2020-12-02

    Whole Foods Recalls Rotisserie Chicken Meals for Undeclared Egg

    Whole Foods Market is recalling Rotisserie Chicken Meals with Mac & Cheese and Broccoli due to a potential undeclared egg allergen. The recall affects specific product codes sold in the Mid-Atlantic region.

    Product
    Rotisserie Chicken Meals with Mac & Cheese and Broccoli, packaged in clear plastic container with printed label product code begins with 261596 261580, 261590, 261601, 261608, or 261616
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0133-2021·2020-12-02

    Whole Foods Chicken Rustico Romano Chef Plate Recalled for Undeclared Egg

    Whole Foods Market is recalling Chicken Rustico Romano Chef Plates due to potential undeclared egg. The product was distributed in five states and Washington, D.C.

    Product
    Chicken Rustico Romano Chef Plate with Mac & Cheese and Broccoli, packaged in clear plastic container with printed label product code begins with 241442
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0138-2021·2020-12-02

    Fresh Express Kit Caesar Supreme Recalled for E. coli O26 Contamination

    Fresh Express is recalling Kit Caesar Supreme salad kits due to potential contamination with Escherichia coli STEC O26.

    Product
    FRESH EXPRESS KIT CAESAR SUPREME, Romaine Lettuce, Creamy Caesar Dressing, Italian Artisan Cheeses, Savory Garlic Croutons, Total Net WT. 10.5oz (298g)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0130-2021·2020-12-02

    Whole Foods Market Recalls Macaroni and Cheese for Undeclared Egg

    Whole Foods Market is recalling specific macaroni and cheese products due to a potential undeclared egg allergen. Consumers in five states and D.C. should check their products.

    Product
    Macaroni & Cheese, chef s case; Macaroni & Cheese, packaged in clear plastic container; Macaroni & Cheese, online and catering product code begins with 286501, 263608, 114449, or 109866
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-0484-2021·2020-12-02

    Hill-Rom Recalls Life2000 Ventilation Systems Due to Fire Risk

    Hill-Rom is recalling 67 Life2000 Ventilation Systems because they pose a risk of fire under certain conditions. The devices are used in home and institutional settings.

    Product
    Life2000 Ventilation System, including Life2000 Ventilator and Life2000 Compressor, Model MS-01-0118 - Product Usage: use in home and institutional settings and is not intended for ambulance or air transport.
    Category
    Medical Device
    Distribution
    Distributed nationwide