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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11176–11200 of 36632

  • SevereNHTSA·20V355000·2020-06-15

    BMW and Toyota Recall Vehicles for Steering Tie Rod Fracture Risk

    BMW and Toyota are recalling specific 2019-2020 models because a steering tie rod may fracture, increasing crash risk. Dealers will replace the parts free of charge.

    Product
    BMW — BMW, TOYOTA X4, 330I, X3, M340I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V356000·2020-06-15

    Blue Bird Recalls 2019-2021 Vision School Buses for Steering Defect

    Blue Bird is recalling 2019-2021 Vision school buses because steering drag link connections may not be tightened, risking loss of control.

    Product
    BLUE BIRD — BLUE BIRD VISION, VISION TRANSIT BUS, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·012-2020·2020-06-13

    Lakeside Refrigerated Services Recalls Ground Beef Due to E. coli O157:H7 Risk

    Lakeside Refrigerated Services is recalling approximately 42,922 pounds of ground beef products that may be contaminated with E. coli O157:H7.

    Product
    Lakeside Refrigerated Services — Lakeside Refrigerated Services Recalls Beef Products due to Possible E.coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V347000·2020-06-12

    Mazda Recalls 2020 CX-30 AWD Vehicles for Fuel Leak Risk

    Mazda is recalling 2020 CX-30 all-wheel drive vehicles because a disconnected fuel hose may leak, increasing fire and crash risks.

    Product
    MAZDA — MAZDA CX-30
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V346000·2020-06-12

    Mazda Recalls 2020 Mazda3 and CX-30 for Brake Caliper Bolt Issue

    Mazda is recalling 2020 Mazda3 and CX-30 vehicles because front brake caliper mounting bolts may not have been tightened properly, which could reduce braking performance.

    Product
    MAZDA — MAZDA MAZDA3, CX-30
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V344000·2020-06-11

    Vermeer Recalls 2020 Wood Chippers Due to Wheel Lug Nut Loosening

    Vermeer is recalling 2020 BC1200XL and BC1500 wood chippers because wheel lug nuts may loosen, allowing the wheel to detach and increasing crash risk.

    Product
    VERMEER — VERMEER BC1500, BC1200XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E038000·2020-06-11

    Dana Heavy Vehicle Output Shafts Recalled for Fracture Risk

    Dana Incorporated is recalling certain heavy vehicle output shafts that may not have been properly heat treated, posing a risk of shaft fracture and detachment.

    Product
    POWER TRAIN:DRIVELINE:DRIVESHAFT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V343000·2020-06-11

    Jeep Cherokee Recall for Power Transfer Unit Spline Wear

    FCA US LLC is recalling 2014-2017 Jeep Cherokee vehicles due to a defect in the Power Transfer Unit that may cause loss of drive or Park function.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E037000·2020-06-11

    Chrysler Recalls Jeep Cherokee Power Transfer Units for Drive Loss Risk

    Chrysler is recalling specific Two-Speed Power Transfer Units for Jeep Cherokee vehicles because worn splines can cause a loss of drive or Park function, increasing crash risk.

    Product
    POWER TRAIN:DRIVELINE:DIFFERENTIAL UNIT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1299-2020·2020-06-10

    Acella Recalls NP Thyroid 15 Tablets Due to Superpotent Drug Risk

    Acella Pharmaceuticals is voluntarily recalling 29,304 bottles of NP Thyroid 15 tablets because the drug is superpotent. The recall covers products distributed nationwide in the US and Puerto Rico.

    Product
    NP THYROID 15 — NP THYROID 15 (LEVOTHYROXINE, LIOTHYRONINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1298-2020·2020-06-10

    Acella Recalls Superpotent NP Thyroid 15 Tablets Nationwide

    Acella Pharmaceuticals is voluntarily recalling 112,140 bottles of NP Thyroid 15 tablets because the drug is superpotent. The recall covers distribution across the US and Puerto Rico.

    Product
    NP THYROID 15 — NP THYROID 15 (LEVOTHYROXINE, LIOTHYRONINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0974-2020·2020-06-10

    KFK Organic Ground Oregano Recalled for Undeclared Tree Nuts and Crustacea

    K F K Seasonings Llc is recalling Organic Ground Oregano due to undeclared tree nuts and Crustacea. The product was distributed in Oregon and Utah.

    Product
    Organic Ground Oregano, Item # 90206. Packaged in 40 lbs. or 50 lbs. cases and sold under brand KFK Seasoning. This product contains Organic Oregano.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Drugs)·D-1300-2020·2020-06-10

    Acella Recalls Superpotent NP Thyroid 15 Thyroid Tablets Nationwide

    Acella Pharmaceuticals is voluntarily recalling 49,128 bottles of NP Thyroid 15 tablets because they are superpotent. The FDA classified this as a Class I recall.

    Product
    NP THYROID 15 — NP THYROID 15 (LEVOTHYROXINE, LIOTHYRONINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0985-2020·2020-06-10

    Sienna Cranberry Orange Muffins Recalled for Undeclared Walnuts

    BAKE'N JOY FOODS, INC. is recalling Sienna brand Cranberry Orange Muffins because they may contain undeclared walnuts.

    Product
    Sienna brand 4.25 oz. Cranberry Orange Muffins coded 20 071 31B
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2219-2020·2020-06-10

    Zimmer Biomet Recalls Vital MIS Spinal Fixation Implants Due to Locking Issues

    Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because the extended tab screws may not lock properly, causing the closure top to back out after surgery.

    Product
    Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 6.5X35MM, Item Number 810M6535 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2210-2020·2020-06-10

    Zimmer Biomet Recalls Vital MIS Spinal Fixation Implants Due to Locking Issues

    Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because the extended tab screws may not lock properly, causing the closure top to back out after surgery.

    Product
    Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 4.5X30MM, Item Number 810M4530 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2205-2020·2020-06-10

    Umano Medical Recalls AC Powered Hospital Adjustable Beds

    Umano Medical is recalling 3,259 AC powered hospital adjustable beds due to a potential hazard of unsupervised patients falling out of bed.

    Product
    AC Powered hospital adjustable bed.
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2261-2020·2020-06-10

    Spacelabs Xhibit Central Recall for Audio Alarm Loss After Power Failure

    Spacelabs Healthcare is recalling Xhibit Central software due to reports of audio alarm loss after power failures or cable disconnections, which could delay alarm recognition.

    Product
    Xhibit Central, Model No. 96102 - Product Usage: intended use is to provide clinicians with central monitoring of adult, pediatric and neonatal patient data of patients connected to networked Spacelabs Healthcare patient monitors and telemetry transmitters.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2206-2020·2020-06-10

    Medtronic Implantable Insulin Pump Recalled for Endotoxin Contamination

    Medtronic is recalling 24 implantable insulin pumps due to endotoxin levels exceeding specifications. The devices were distributed only in the Netherlands, France, and Sweden.

    Product
    Medtronic Implantable Insulin Pump System, REF: MMT-2007D, Sterile EO, CE 0459 UDI: 00763000043001
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2258-2020·2020-06-10

    GE Healthcare Recalls Nuclear Medicine Systems Due to Software Defect

    GE Healthcare is recalling 526 Nuclear Medicine systems because outdated software caused a patient's finger to be injured during an automatic unload process.

    Product
    System, Tomography Computed Emmission
    Category
    Medical Device
    Distribution
    40 states
  • SevereFDA (Food)·F-0972-2020·2020-06-10

    K F K Seasonings Recalls Azure Market Chili Powder for Undeclared Allergens

    K F K Seasonings LLC is recalling 96 lbs of Azure Market Chili Powder, Mild, Organic due to undeclared tree nuts and Crustacea.

    Product
    Chili Powder, Mild, Organic is a blend, Item # 90030. Packaged in 1 lb. bags and sold under brand Azure Market. This product contains "Organic Chili Peppers, Salt, Organic Spices, Organic Garlic, Organic Sunflower Oil". The Azure Market label listed the lot # 90030041520 and…
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2257-2020·2020-06-10

    Siemens ARTIS icono X-Ray Systems Recalled for Incorrect Vessel Quantification

    Siemens is recalling five ARTIS icono X-ray systems because software may fail to detect vessels or provide incorrect measurements, potentially leading to wrong diagnoses.

    Product
    ARTIS icono systems with Quantification Application SW (QVA/QCA) on a standalone XWP computer, an interventional Fluoroscopic X-Ray System Model Number: 11327600
    Category
    Medical Device
    Distribution
    4 states