The Recall Desk

Severity 4 of 5

Severe recalls

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

12676–12700 of 29171

  • SevereFDA (Drugs)·D-0988-2019·2019-03-13

    Sunstone Organics Recalls White Vein Kratom Capsules Due to Salmonella

    Sunstone Organics is recalling White Vein Kratom capsules in 20, 60, and 150-count bottles because samples tested positive for Salmonella.

    Product
    White Vein Kratom, packaged in a) 20 count capsules (UPC 00859667007347), b) 60 count capsules (UPC 00859667007354), c) 150 count capsules (UPC 00859667007361), Sunstone Organics Springfield, Oregon 97473 541-972-3327.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1148-2019·2019-03-13

    Stacy's Pita Chips Recalled for Potential Undeclared Milk

    Frito-Lay is recalling Stacy's Simply Naked Pita Chips due to a potential undeclared milk allergen. Consumers should check their bags for specific dates and codes.

    Product
    Stacy's Simply Naked Pita Chips 7 1/3 ounce bags
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0520-2019·2019-03-13

    Vi-Jon Hydrogen Peroxide Recalled for IPA Contamination

    Vi-Jon, Inc. is recalling 32-ounce bottles of Hydrogen Peroxide First Aid Antiseptic due to the presence of Isopropyl Alcohol (IPA). The product was distributed in Ohio.

    Product
    Topical Solution USP Hydrogen Peroxide First Aid Antiseptic Oral Debriding Agent 32 Fl. Oz. (1 QT) 946 mL bottle, Distributed By: Discount Drug Mart 211 Commerce Drive, Medina, Ohio 44256 NDC 53943-871-45 UPC 0-93351-12758-8
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-1141-2019·2019-03-13

    Southwind Foods Recalls Wild Dungeness Crab Cake Due to Temperature Abuse

    Southwind Foods is recalling 13 cases of Wild Dungeness Crab Cake sold at Whole Foods in California, Arizona, and Hawaii due to potential temperature abuse.

    Product
    Wild Dungeness Crab Cake; Net Weight: 12 lb - 48 x 4.0 oz. Keep Frozen Manufactured for Whole Foods Market
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0986-2019·2019-03-13

    Sunstone Organics Recalls Maeng Da Kratom Powder Due to Salmonella Contamination

    Sunstone Organics is recalling Maeng Da Kratom powder in 25, 50, and 100-gram packages due to positive Salmonella test results.

    Product
    Maeng Da Kratom, packaged in a) 25 gram powder (UPC 00859667007118), b) 50 gram powder (UPC 00859667007125), c) 100 gram powder (UPC 00859667007132), Sunstone Organics Springfield, Oregon 97473, 541-972-3327.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1171-2019·2019-03-13

    Kingston Pharma Recalls DG Baby Gripe Water Due to Undissolved Ingredient

    Kingston Pharma LLC is recalling DG Baby Gripe Water herbal supplements because they contain an undissolved ingredient, citrus flavonoid.

    Product
    DG Baby Gripe Water herbal supplement with organic ginger and fennel extracts, 4 FL OZ (120 mL) Liquid Dietary Supplement UPC: 8 54954 00246 3
    Category
    Food
    Distribution
    43 states
  • SevereFDA (Drugs)·D-0987-2019·2019-03-13

    Sunstone Organics Recalls White Vein Kratom Powder Due to Salmonella

    Sunstone Organics is recalling White Vein Kratom powder in 25, 50, and 100-gram packages because samples tested positive for Salmonella.

    Product
    White Vein Kratom, packaged in a) 25 gram powder (UPC 00859667007316), b) 50 gram powder (UPC 00859667007323), c) 100 gram powder (UPC 00859667007330), Sunstone Organics Springfield, Oregon 97473, 541-972-3327.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0988-2019·2019-03-13

    Maquet XS Flat Screen Monitor Holder Recalled for Grounding Defect

    Getinge is recalling six Maquet XS Flat Screen Monitor Holders in Arizona and Texas because they may not meet grounding requirements, posing a risk of electric shock.

    Product
    Maquet XS Flat Screen Monitor Holder, PWD50+DF XS32 K3 SPE, Configuration Part Number ARD268400140A Product Usage: This product is designed to support one or two medical grade flat screen(s) alone or in association with surgical lights.
    Category
    Medical Device
    Distribution
    2 states
  • SevereNHTSA·19V197000·2019-03-13

    Newmar Recalls 2017-2019 Ventana Motorhomes for Loose Steering Bolts

    Newmar is recalling 2017-2019 Ventana motorhomes because loose steering and tie rod arm bolts may separate, causing loss of vehicle control and increasing crash risk.

    Product
    NEWMAR — NEWMAR VENTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19079·2019-03-12

    HP Recalls Lithium-Ion Batteries for Commercial Notebooks and Workstations

    HP is expanding a recall of lithium-ion batteries for commercial notebook computers and mobile workstations due to fire and burn hazards.

    Product
    Lithium-ion batteries for HP commercial notebook computers and mobile workstations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E024000·2019-03-11

    Natural Gas Fuel Systems Recalls CNG Fuel Cylinders for Rupture Risk

    Natural Gas Fuel Systems is recalling specific compressed natural gas fuel systems for heavy and medium-duty vehicles because the cylinders may unexpectedly rupture.

    Product
    FUEL SYSTEM, OTHER:STORAGE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V195000·2019-03-11

    Mertz Custom Trailer Recall for Air Brake Plastic Connector Defect

    Mertz is recalling 2008-2018 custom trailers because plastic air brake connectors may fail, potentially causing brake loss or unexpected emergency brake activation.

    Product
    MERTZ — MERTZ CUSTOM TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·025-2019·2019-03-09

    Conagra Recalls Chef Boyardee Bowls Due to Undeclared Allergens and Misbranding

    Conagra Brands is recalling specific Chef Boyardee rice bowls that contain undeclared milk and wheat allergens and are mislabeled as beef ravioli.

    Product
    Hometown Food Company — Conagra Brands, Inc. Recalls Chicken and Rice Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·19V194000·2019-03-08

    SVO Group Recalls 2018 Embassy Buses for Rear Axle Defect

    SVO Group is recalling 2018 Embassy shuttle buses because loose U-bolts may allow the rear axle to separate, increasing crash risk.

    Product
    SVO GROUP — SVO GROUP EMBASSY BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V186000·2019-03-08

    EBY Livestock Trailer Recall for Improperly Greased Axle Bearings

    M H EBY is recalling 2019-2020 EBY Gooseneck Livestock Trailers because inner wheel bearings may not have been properly greased, posing fire and crash risks.

    Product
    EBY — EBY RUFF NECK, WRANGLER, MAVERICK, MAVERICK LS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V187000·2019-03-07

    Suzuki Recalls Grand Vitara and Kizashi for Air Bag Sensor Issues

    Suzuki is recalling 2006-2013 Grand Vitara and 2010-2013 Kizashi vehicles because the front passenger seat may shrink, causing the air bag sensor to misclassify occupants.

    Product
    SUZUKI — SUZUKI GRAND VITARA, KIZASHI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0906-2019·2019-03-06

    Philips Achieva 3.0T MRI System Recalled for Ceiling Speaker Hazard

    Philips is recalling 11,226 Achieva 3.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva 3.0T TX-series, Model Number 781278. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1103-2019·2019-03-06

    Whole Foods Mediterranean Stuffed Salmon Recalled for Salmonella Risk

    Whole Foods Market is recalling Mediterranean Stuffed Salmon in plastic containers due to potential Salmonella contamination. The product was sold in eight Northeastern and Southeastern states.

    Product
    Mediterranean Stuffed Salmon packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0907-2019·2019-03-06

    Philips Achieva MRI System Recalled for Falling Ceiling Speaker Hazard

    Philips is recalling Achieva 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva 1.5T Conversion, Model Number 781283. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0922-2019·2019-03-06

    Philips Ingenia Elition S MRI System Recalled for Falling Speaker Hazard

    Philips is recalling Ingenia Elition S MRI systems because ceiling speakers may fall due to magnetic attraction.

    Product
    Ingenia Elition S, Model Number 781357. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0878-2019·2019-03-06

    Philips MRI System Recall Due to Ceiling Speaker Magnetic Hazard

    Philips is recalling Intera 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Intera 1.5T Power/Pulsar, Model Number 781105. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1126-2019·2019-03-06

    Whole Foods Recalls Spinach Artichoke Bleus Pizza Due to Salmonella Risk

    Whole Foods Market is recalling Spinach Artichoke Bleus Pizza packaged in plastic nonflexible containers because the product is potentially contaminated with Salmonella.

    Product
    Spinach Artichoke Bleus Pizza packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0886-2019·2019-03-06

    Philips Intera 1.5T MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling 11,226 Intera 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Intera 1.5T R11, Model Number 781170. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide