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.

12726–12750 of 29186

  • SevereFDA (Devices)·Z-0927-2019·2019-03-06

    Philips Achieva 3.0T MRI System Recalled for Ceiling Speaker Hazard

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

    Product
    Achieva 3.0T for PET, Model Number 781477. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1122-2019·2019-03-06

    Whole Foods Spinach and Mushroom Salad Recalled for Salmonella Risk

    Whole Foods Market is recalling Large and Small Spinach and Mushroom Salads due to potential Salmonella contamination. The products were sold in eight northeastern and southeastern states.

    Product
    Large Spinach and Mushroom Salad and Small Spinach and Mushroom Salad packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0923-2019·2019-03-06

    Philips Ingenia Elition X MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling Ingenia Elition X MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Ingenia Elition X, Model Number 781358. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0893-2019·2019-03-06

    Philips Achieva 3.0T MRI System Recalled Due to 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, Model Number 781177. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0926-2019·2019-03-06

    Philips MR RT MRI Systems Recalled for Falling Ceiling Speaker Hazard

    Philips is recalling MR RT MRI systems because ceiling speakers may fall due to magnetic attraction.

    Product
    MR RT, Model Number 781439. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V188000·2019-03-06

    Volkswagen Recalls 56,173 Vehicles for Rear Coil Spring Fracture Risk

    Volkswagen is recalling 56,173 vehicles because rear coil springs may fracture prematurely, potentially causing tire damage and loss of vehicle control.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN, GOLF SPORTWAGEN, GOLF, JETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V178000·2019-03-06

    Entegra Recalls 2019-2020 Reatta Motorhomes for Damaged Tow Hitch

    Entegra Coach is recalling 2019-2020 Reatta motorhomes because the tow hitch may have been damaged during delivery, increasing the risk of a crash.

    Product
    ENTEGRA — ENTEGRA REATTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0895-2019·2019-03-06

    Philips Intera 1.5T MRI System Recalled for Ceiling Speaker 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, Model Number 781195. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1091-2019·2019-03-06

    Produce Packaging Inc. Recalls Stir-Fry Mix Due to E. coli Risk

    Produce Packaging Inc. is recalling 525 units of 9 LB Stir-Fry Mix due to potential E. coli contamination. The product was distributed in Ohio, Michigan, New York, and Texas.

    Product
    Produce Packaging, Inc. Mix, Stir-Fry WG 9 LB
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0873-2019·2019-03-06

    Philips Multiva MRI System Recalled Due to Ceiling Speaker Hazard

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

    Product
    Multiva 1.5T 16 R5, Model Number 781078. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1104-2019·2019-03-06

    Whole Foods Quinoa with Dark Leafy Greens Recalled for Salmonella Risk

    Whole Foods Market is recalling Quinoa with Dark Leafy Greens due to potential Salmonella contamination. The product was sold in eight northeastern and southeastern states.

    Product
    Quinoa with Dark Leafy Greens packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0876-2019·2019-03-06

    Philips Intera 1.0T MRI System Recalled for Ceiling Speaker Hazard

    Philips is recalling Intera 1.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Intera 1.0T Power/Pulsar, Model Number 781103. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V177000·2019-03-06

    Jayco Recalls 2019-2020 Embark Motorhomes Due to Hitch Damage

    Jayco is recalling 2019-2020 Embark motorhomes because the hitch may have been damaged during delivery, increasing the risk of a crash if the towed vehicle separates.

    Product
    JAYCO — JAYCO EMBARK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1116-2019·2019-03-06

    Whole Foods Recalls Breakfast Sandwich Platters Due to Salmonella Risk

    Whole Foods Market is recalling Breakfast Sandwich Platters packaged in plastic nonflexible containers due to potential Salmonella contamination.

    Product
    Breakfast Sandwich Platter packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-1121-2019·2019-03-06

    Whole Foods Market Recalls Large Goat Cheese Green Salad for Salmonella Risk

    Whole Foods Market is recalling Large Goat Cheese Green Salad due to potential Salmonella contamination. The product was sold in eight northeastern and southeastern states.

    Product
    Large Goat Cheese Green Salad packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0915-2019·2019-03-06

    Philips Achieva 1.5T MRI System Recalled for Falling Speaker Hazard

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

    Product
    Achieva 1.5T Conversion, Model Number 781346. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0901-2019·2019-03-06

    Philips Ingenia MRI System Recalled Due to Ceiling Speaker Hazard

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

    Product
    Ingenia 1.5T CX, Model Number 781261. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0918-2019·2019-03-06

    Philips Ingenia 3.0T MRI System Recalled for Falling Speaker Hazard

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

    Product
    Ingenia 3.0T, Model Number 781377. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1107-2019·2019-03-06

    Whole Foods Spinach Ravioli Salad Recalled for Salmonella Risk

    Whole Foods Market is recalling Spinach Ravioli Salad with Lemon, Tomato, and Parmesan due to potential Salmonella contamination.

    Product
    Spinach Ravioli Salad with Lemon, Tomato, and Parmesan packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0916-2019·2019-03-06

    Philips Ingenia 1.5T S MRI Systems Recalled for Falling Speaker Hazard

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

    Product
    Ingenia 1.5T S, Model Number 781347. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0885-2019·2019-03-06

    Philips Intera IT MRI Systems Recalled for Falling Ceiling Speaker Risk

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

    Product
    Intera IT, Model Number 781160. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide