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.

16601–16625 of 29206

  • SevereFDA (Devices)·Z-1133-2017·2017-02-08

    Medtronic Intact Disposable Wands Recalled for Sterility Compromise

    Medtronic is recalling Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The recall covers 275 units distributed worldwide.

    Product
    Intact Disposable Wands (part of the Intact System) 900-120: 5 Pack 20mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·011-2017·2017-02-07

    Ukrop's Recalls Chili Flavored Soups Due To Undeclared Allergens

    Ukrop's Homestyle Foods is recalling approximately 45 pounds of beef and chicken chili flavored soups because they contain undeclared milk, wheat, and soy.

    Product
    Ukrop's Homestyle Foods — Ukrop’s Homestyle Foods Recalls Beef and Chicken Chili Flavored Soup Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·17V070000·2017-02-03

    Volkswagen Recalls 2017 Jetta Vehicles Due to Engine Seizure Risk

    Volkswagen is recalling 2017 Jetta vehicles with 1.4L engines because the engine block may be improperly cast, potentially causing the engine to seize and leading to a loss of vehicle control.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V072000·2017-02-03

    REV Recalls 2016-2017 Motorhomes Due to Fuel Leak Risk

    REV Recreation Group is recalling 391 Holiday Rambler and Fleetwood motorhomes because a spring shackle bolt may puncture fuel components, creating a fire hazard.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD VACATIONER XE, STORM, VACATIONER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17081·2017-02-02

    Disney Recalls Mickey Mouse Nightlights Due to Fire Hazard

    Walt Disney Parks and Resorts is recalling Happy Holidays! Mickey Mouse Nightlights because liquid can leak onto electrical outlets, posing a fire hazard.

    Product
    Happy Holidays! Mickey Mouse Nightlights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V067000·2017-02-02

    BMW Recalls 2011-2012 Models for Rear Driveshaft CV Joint Defect

    BMW is recalling specific 2011-2012 models because the rear driveshaft CV joint may break, causing loss of propulsion and increasing crash risk.

    Product
    BMW — BMW 335I, Z4, 335D, 535I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0923-2017·2017-02-01

    Philips Allura Xper FD10 X-ray System Recalled for Loose Screws

    Philips is recalling one Allura Xper FD10 X-ray system because production errors left screws loose, potentially causing the C-arm to rotate uncontrolled.

    Product
    Allura Xper FD10 722026 is intended for: Cardiovascular and vascular X-ray imaging applications, including diagnostic, interventional procedures (such as PTCA, stent placement and atherectomies), pacemaker implantations and Electro Physiology(EP).
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Food)·F-1345-2017·2017-02-01

    SYNEDREX Weight Loss Solution Recalled for Unapproved Ingredients

    IQ Formulations is recalling SYNEDREX weight loss capsules because they contain Picamilon and/or methylpentane citrate, which are not recognized as dietary ingredients.

    Product
    SYNEDREX, Powerful stimulant weight loss solution, 45 capsules (UPC 764779-224592). Brand: Metabolic Nutrition.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1305-2017·2017-02-01

    Dutch-American Foods Recalls White Chocolate Mousse for Salmonella Risk

    Dutch-American Foods is recalling 1-Step White Chocolate Mousse due to potential Salmonella contamination. Consumers in MD, MI, IL, and FL should stop using the product.

    Product
    1-Step White Chocolate Mousse, NET WEIGHT: 1 BAG: 35 oz/ 1 kg
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-1065-2017·2017-02-01

    Villa Radiology Systems Recalls Apollo DRF X-Ray Systems Due to Injury Risk

    Villa Radiology Systems LLC is recalling 66 Apollo DRF multi-function x-ray systems because a chain of faults led to an injury involving inadvertent movement activation.

    Product
    Apollo DRF: Model: 9784220831 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.
    Category
    Medical Device
    Distribution
    26 states
  • SevereNHTSA·17V065000·2017-02-01

    Highland Ridge Recalls 2016-2017 Open Range Fifth-Wheels for Axle Defect

    Highland Ridge RV is recalling 2016-2017 Open Range fifth-wheel vehicles because axle hangers may puncture the riser tube, causing axle misalignment and tire failure.

    Product
    HIGHLAND RIDGE FW — HIGHLAND RIDGE FW OPEN RANGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1350-2017·2017-02-01

    IQ Formulations Recalls Pre-Workout Powder Containing Unapproved Ingredients

    IQ Formulations is recalling P.S.P. Pre-Workout powder because it contains Picamilon and/or methylpentane citrate, which are not recognized as dietary ingredients.

    Product
    P.S.P., Pre-Workout, Physique Stimulating Pre-workout, Powder, 360 g, watermelon flavor (UPC 764779-360450). Brand: Metabolic Nutrition
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1303-2017·2017-02-01

    Dutch-American Foods Recalls Creamy Ranch Seasoning for Salmonella Risk

    Dutch-American Foods is recalling Creamy Ranch seasoning products due to potential Salmonella contamination. The recall affects 70 bags distributed in Maryland, Michigan, Illinois, and Florida.

    Product
    Creamy Ranch, Net Wt. 50 lbs (22.73 kg), Item Number 16131505
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1337-2017·2017-02-01

    Victory General Foods Recalls Elder Paintsil's GA Kenkey for Insanitary Conditions

    Victory General Foods is recalling Elder Paintsil's GA Kenkey because it was manufactured under insanitary conditions and without following required food code processes.

    Product
    ELDER PAINTSIL'S GA KENKEY, NET WT. 1.20, UPC: 6 61799 58166 0, MANUFACTURED BY VICTORY GENERAL FOODS IN WORCESTER, MA 01603
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1351-2017·2017-02-01

    Metabolic Nutrition Pre-Workout Powder Recalled for Unapproved Ingredients

    IQ Formulations is recalling Metabolic Nutrition P.S.P. Pre-Workout powder because it contains Picamilon and/or methylpentane citrate, which are not recognized as dietary ingredients.

    Product
    P.S.P., Pre-Workout, Physique Stimulating Pre-workout, Powder, 360 g, blue raspberry (UPC 764779-360122). Brand: Metabolic Nutrition.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1063-2017·2017-02-01

    Villa Radiology Juno DRF X-ray Systems Recalled for Injury Risk

    Villa Radiology Systems LLC is recalling Juno DRF x-ray systems after an injury occurred due to a chain of faults involving physical barriers and labeling.

    Product
    Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.
    Category
    Medical Device
    Distribution
    26 states
  • SevereFDA (Devices)·Z-0925-2017·2017-02-01

    Philips Allura Xper FD20/15 C-arm Recall Due to Loose Screws

    Philips is recalling two Allura Xper FD20/15 systems because production errors may cause C-arm screws to loosen, leading to uncontrolled rotation.

    Product
    Allura Xper FD20/15 R8.2 722058 is intended for: Cardiovascular and vascular X-ray imaging applications, including diagnostic, interventional procedures (such as PTCA, stent placement and atherectomies), pacemaker implantations and Electro Physiology(EP).
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1064-2017·2017-02-01

    Villa Radiology Systems Recalls Apollo X-Ray Systems Due to Injury Risk

    Villa Radiology Systems LLC is recalling 66 Apollo multi-function x-ray systems after an injury incident involving inadvertent movement activation and delayed emergency stop response.

    Product
    Apollo: Models: 9784000131, 9784000231, 9784020131, 9784020231, 9784100231, 9784120131, 9784120231, 9784130131 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.
    Category
    Medical Device
    Distribution
    26 states
  • SevereFDA (Food)·F-1357-2017·2017-02-01

    Berner Creamy Alfredo Pasta Sauce Recalled for Bacterial Contamination

    Berner Food & Beverage is recalling Creamy Alfredo Pasta Sauce contaminated with spoilage bacteria. Consumers should stop using the product.

    Product
    Creamy Alfredo, Pasta Sauce; NET WT. 15 OZ, CONT. NET 425g; Glass jar, metal lid; UPC 41220845941, 70038626695 or 041498172855
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Devices)·Z-0924-2017·2017-02-01

    Philips Allura Xper FD20 C-arm Recall Due to Loose Screws

    Philips is recalling two Allura Xper FD20 C-arm systems because production errors left screws loose, posing a risk of uncontrolled rotation.

    Product
    Allura Xper FD20 R8.2 722028 is intended for: Cardiovascular and vascular X-ray imaging applications, including diagnostic, interventional procedures (such as PTCA, stent placement and atherectomies), pacemaker implantations and Electrophysiology(EP).
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Food)·F-1346-2017·2017-02-01

    IQ Formulations Recalls E.S.P. Pre-Workout Powder for Unapproved Ingredients

    IQ Formulations is recalling E.S.P. Pre-Workout powder because it contains picamilon and/or methylpentane citrate, which are not recognized as dietary ingredients.

    Product
    E.S.P. Pre-Workout, Energy Stimulant Pre-workout, Powder, 300 g, Watermelon flavor (UPC 764779-4407566). Brand: Metabolic Nutrition.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1099-2017·2017-02-01

    Roche Recalls Accu-Chek Connect App Due to Insulin Dosing Errors

    Roche Diabetes Care is recalling the Accu-Chek Connect app because software defects may cause incorrect insulin bolus recommendations, potentially leading to hypoglycemia.

    Product
    Accu-Chek Connect Diabetes Management App
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1306-2017·2017-02-01

    Dutch-American Foods Recalls White Chocolate Mousse for Salmonella Risk

    Dutch-American Foods is recalling 2-Step White Chocolate Mousse due to potential Salmonella contamination. The product was distributed in Maryland, Michigan, Illinois, and Florida.

    Product
    2-Step White Chocolate Mousse, NET WEIGHT: 1 BAG: 35 oz/ 1 kg
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1301-2017·2017-02-01

    Dutch-American Foods Recalls Butter Popcorn Seasoning for Salmonella Risk

    Dutch-American Foods is recalling CCF Butter Popcorn Seasoning due to potential Salmonella contamination. The product was distributed in Maryland, Michigan, Illinois, and Florida.

    Product
    CCF Butter Popcorn Seasoning, NET Wt. 1000 lbs, Gluten Free
    Category
    Food
    Distribution
    4 states