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.

14726–14750 of 29202

  • SevereFDA (Devices)·Z-0713-2018·2018-03-07

    Siemens SOMATOM Go.Up CT Table Recall for Potential Instability

    Siemens Medical Solutions is recalling six SOMATOM Go.Up CT system tables because improperly tightened bolts may loosen, causing the table to become unstable.

    Product
    SOMATOM Go.Up computed tomography (CT) x-ray system table, Model Number: 11061628 Product Usage: Intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by these systems can be used by a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0715-2018·2018-03-07

    Mobius AIRO Mobile CT System Recalled for Unintended Motion Risk

    Mobius Imaging is recalling 105 AIRO Mobile CT Systems due to a risk of unintended device motion during startup or scan preparation.

    Product
    AIRO Mobile CT System, Model Number: MobiCT-32 Product Usage: The AIRO¿ is intended to be used for X-ray computed tomography applications for anatomy that can be imaged in the 107cm aperture excluding pediatric patients and patients weighing over 400 lbs. (182 kg).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0831-2018·2018-03-07

    Sumano's Bakery Recalls Sourdough Baguettes Due to Metal Contamination

    Sumano's Bakery is recalling Sourdough Baguettes because a customer found a small metal piece on the outside of the bread before baking.

    Product
    Sourdough Baguette: Product number 2064; SKU 61659798; GTIN [00046567600949]; UPC 831 49000064 20 pieces; Ingredients: Unbleached Wheat Flour, Water, Sea Salt, Starter (Fermented dough). Best Practices: 1. Keep Bread frozen at all times 2. Pull bread out of freezer…
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0733-2018·2018-03-07

    Ventana ultraView SISH DNP Detection Kit Recalled for Leaking Reagent Dispensers

    Ventana Medical Systems is recalling 20 units of the ultraView SISH DNP Detection Kit due to increased reports of leaking and sticking reagent dispensers.

    Product
    ultraView SISH DNP Detection Kit US, Ventana Part Number 760-098, Roche GMMI 05572037001 in vitro diagnostic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0730-2018·2018-03-07

    Ventana ultraView Universal DAB Detection Kit Recalled for Leaking Reagent Dispensers

    Ventana Medical Systems is recalling ultraView Universal DAB Detection Kits due to increased reports of leaking and sticking reagent dispensers.

    Product
    ultraView Universal DAB Detection Kit, Ventana part Number 760-500, Roche GMMI 05269806001 in vitro diagnostic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0714-2018·2018-03-07

    Siemens CT Table Recalled Due to Potential Bolt Loosening and Instability

    Siemens Medical Solutions is recalling SOMATOM Go.Now CT system tables because bolts may loosen, causing the table to become unstable.

    Product
    SOMATOM Go.Now computed tomography (CT) x-ray system table, Model Number: 11061618 Product Usage: Intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by these systems can be used by a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V150000·2018-03-06

    Mercedes-Benz Recalls 2018 AMG Models for Seat Welding Defect

    Mercedes-Benz is recalling 2018 AMG C43, C63S, and E63S vehicles because improperly welded seat backrests may fail in a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG E63S, AMG C63S, AMG C43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V148000·2018-03-06

    Volkswagen Recalls Vehicles Due to Driver Air Bag Inflator Explosion Risk

    Volkswagen is recalling specific 2007-2014 models because the driver's frontal air bag inflator may explode during deployment, potentially causing serious injury or death.

    Product
    VOLKSWAGEN — VOLKSWAGEN GOLF, PASSAT, CC, EOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V149000·2018-03-06

    RAM ProMaster City Recall for Steering Gear Casting Defect

    Chrysler is recalling 2018 RAM ProMaster City vehicles because a casting defect in the steering system may cause fluid leaks and increased steering effort.

    Product
    RAM — RAM PROMASTER CITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V152000·2018-03-06

    Mack Trucks Recalls 2018 Models Due to Electrical Overload Risk

    Mack Trucks is recalling 2018 Anthem, Granite, and Pinnacle trucks because an electrical overload may cause the light control module to fail, potentially disabling exterior lights and windshield wipers.

    Product
    MACK — MACK GRANITE (GU), PINNACLE (CXU), PINNACLE (PI/PN), ANTHEM (AN)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·019-2018·2018-03-03

    Interstate Meat Distributors Recalls Ground Beef and Pork for E. coli Risk

    Interstate Meat Distributors is recalling approximately 14,806 pounds of ground beef and pork products due to possible E. coli O157:H7 contamination.

    Product
    Interstate Meat Dist., Inc. — Interstate Meat Distributors, Inc., Recalls Ground Beef and Pork Products due to Possible E. coli O157:H7 Contamination
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·18V143000·2018-03-02

    Keystone Recalls 2018 Recreational Trailers Due to Propane Leak Risk

    Keystone is recalling 2,958 specific 2018 recreational trailers because a loose propane valve screw may cause gas leaks and fire.

    Product
    DUTCHMEN — DUTCHMEN, KEYSTONE, CROSSROADS ASPEN TRAIL, PASSPORT, ZINGER, HIDEOUT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·18110·2018-03-01

    Double Insight Recalls Gem 65 Multicookers Due to Fire Hazard

    Double Insight is recalling Gem 65 8-in-1 multicookers sold at Walmart because a defect can cause the unit to overheat and melt, posing a fire hazard.

    Product
    Gem 65 8-in-1 multicookers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V140000·2018-03-01

    Jaguar Recalls 2018 E-Pace Vehicles Due to Front Brake Hose Bracket Defect

    Jaguar is recalling 2018 E-Pace vehicles because improperly installed front brake hose brackets may allow hoses to contact tires, causing fluid leaks and increased stopping distances.

    Product
    JAGUAR — JAGUAR E-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·015-2018·2018-03-01

    Sensenig Turkey Farm Recalls Turkey Sausage for Undeclared Allergens

    Sensenig Turkey Farm LLC is recalling approximately 1,925 pounds of raw turkey sausage products because they contain undeclared wheat and soy allergens.

    Product
    Sensenig Turkey Farm LLC — Sensenig Turkey Farm LLC Recalls Turkey Sausage Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0642-2018·2018-02-28

    Allen Medical Systems Recalls Radiolucent Surgery Spine Frames

    Allen Medical Systems is recalling 161 Radiolucent Surgery Spine Frames because the base may crack during patient transfer.

    Product
    Radiolucent Surgery Spine Frame (F70801). Surgical platform used to position patients for lumbar spine procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0453-2018·2018-02-28

    Pharmedium Recalls Ropivacaine HCl Injection Due to Sterility Assurance Concerns

    Pharmedium Services, LLC is recalling all lots of Ropivacaine HCl in 0.9% Sodium Chloride due to a lack of sterility assurance. The recall covers all strengths, doses, and packaging nationwide.

    Product
    Ropivacaine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0443-2018·2018-02-28

    Pharmedium Recalls Adenosine Injection Due to Sterility Assurance Concerns

    Pharmedium Services, LLC is recalling all lots of Adenosine Injection because of a lack of sterility assurance. The recall covers products distributed nationwide.

    Product
    Adenosine Injection in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0465-2018·2018-02-28

    Pharmedium Recalls Meperidine HCl Injections Due To Sterility Concerns

    Pharmedium Services, LLC is recalling Meperidine HCl in 0.9% Sodium Chloride injections nationwide due to a lack of sterility assurance.

    Product
    Meperidine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0441-2018·2018-02-28

    Pharmedium Recalls Ketamine HCl Injection Due to Sterility Assurance Concerns

    Pharmedium Services, LLC is recalling all lots of Ketamine HCl in 0.9% Sodium Chloride due to a lack of sterility assurance. The recall covers all strengths, doses, and packaging nationwide.

    Product
    Ketamine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0466-2018·2018-02-28

    Pharmedium Recalls Methadone HCl Injection Due to Sterility Concerns

    Pharmedium Services, LLC is recalling Methadone HCl Injection in all strengths and packaging due to a lack of sterility assurance.

    Product
    Methadone HCl Injection in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0460-2018·2018-02-28

    Pharmedium Recalls Labetalol HCl Infusions Due to Sterility Assurance Concerns

    Pharmedium Services, LLC is recalling Labetalol HCl in 0.9% Sodium Chloride infusions nationwide due to a lack of sterility assurance.

    Product
    Labetalol HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide