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.

17851–17875 of 29217

  • SevereNHTSA·16V614000·2016-08-23

    Land Rover Recalls Vehicles for Transmission Shift to Neutral Risk

    Land Rover is recalling certain 2014-2015 Range Rover Evoque and 2015 Discovery Sport vehicles because the transmission may unexpectedly shift to neutral, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER EVOQUE, DISCOVERY SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V610000·2016-08-22

    Zero Motorcycles Recalls 2015 Models Due to ABS Failure Risk

    Zero Motorcycles is recalling 96 model year 2015 SR, S, DS, and FX motorcycles because a faulty DC-DC converter may cause the anti-lock brake system and lights to stop working.

    Product
    ZERO — ZERO SR, S, DS, FX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1898-2016·2016-08-17

    Let's Do Lunch Recalls Beef Burger Patties for Listeria Risk

    Let's Do Lunch, Inc. is recalling Integrated Food Service All America Burger Beef Patties due to potential Listeria monocytogenes contamination.

    Product
    Integrated Food Service All America Burger Beef Patty on a Whole Grain Bun Code #470007
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1906-2016·2016-08-17

    Let's Do Lunch Recalls Chili Cheese Dogs for Listeria Risk

    Let's Do Lunch, Inc. is recalling Integrated Food Service Chili Cheese Dogs on Whole Grain Buns due to potential Listeria monocytogenes contamination.

    Product
    Integrated Food Service Chili Cheese Dog on Whole Grain Buns Code #809022
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1907-2016·2016-08-17

    Let's Do Lunch Recalls Chicken Little Sliders for Listeria Risk

    Let's Do Lunch, Inc. is recalling Integrated Food Service Chicken Little Sliders-Wrapped due to potential Listeria monocytogenes contamination.

    Product
    Integrated Food Service Chicken Little Sliders-Wrapped Code #809050
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1909-2016·2016-08-17

    Let's Do Lunch Recalls Chicken Hot Dog for Listeria Risk

    Let's Do Lunch, Inc. is recalling Integrated Food Service Chicken Hot Dog on a Whole Grain Bun due to potential Listeria monocytogenes contamination.

    Product
    Integrated Food Service Chicken Hot Dog on a Whole Grain Bun Code #941500
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1896-2016·2016-08-17

    Let's Do Lunch Recalls Chicken Patty Sandwiches for Listeria Risk

    Let's Do Lunch, Inc. is recalling Integrated Food Service Chicken Patty Sandwiches due to potential Listeria monocytogenes contamination.

    Product
    Integrated Food Service Chicken Patty Sandwich Chicken Patty on a Whole Grain Bun Code #400003
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1921-2016·2016-08-17

    Raw Refrigerated Cucumbers Recalled Due to Salmonella Contamination

    Maglio & Co Ready Fresh is recalling raw refrigerated cucumbers because a sample tested positive for Salmonella spp.

    Product
    Raw Refrigerated Cucumbers, 11/9 bushel, 6 count, 12 count, 24 count, in corrugated cardboard cases, Southern Valley Produce Lot 16300705. (The product was either distributed in original container or were repackaged).
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-1455-2016·2016-08-17

    Teva Recalls Albuterol Sulfate Syrup Due to Foreign Particles

    Teva North America is recalling 8,052 bottles of Albuterol Sulfate Syrup because black particles were found in the product.

    Product
    Albuterol Sulfate Syrup, 2 mg/ 5 mL, 473 mL bottle, Rx only, Manufactured in Canada by Contract Pharmaceuticals Limited, Canada, Manufactured For: Teva Pharmaceuticals USA, Sellersville, PA --- NDC 0093-0661-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1456-2016·2016-08-17

    Spectrum Chemical Recalls Zinc Acetate Due to Excess Lead Levels

    Spectrum Laboratory Products is recalling Zinc Acetate, Crystal, USP, because it contains lead levels exceeding USP monograph limits.

    Product
    Zinc Acetate, Crystal, USP, packaged in 500 gram bottles, Spectrum Chemical MFG, CORP., New Brunswick, NJ 08901
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Food)·F-1889-2016·2016-08-17

    Let's Do Lunch Recalls Italian Submarine Sandwiches for Listeria Risk

    Let's Do Lunch, Inc. is recalling Integrated Food Service Italian Submarine Sandwiches due to potential Listeria monocytogenes contamination. The products were distributed nationwide.

    Product
    Integrated Food Service Italian Submarine Sandwich Code #C140004/C14004
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1877-2016·2016-08-17

    Let's Do Lunch Recalls Turkey Ham & Cheese Deli Flatz for Listeria Risk

    Let's Do Lunch, Inc. is recalling Cafe Favorites Turkey Ham & Cheese Deli Flatz due to potential Listeria monocytogenes contamination. The product was distributed nationwide in the U.S.

    Product
    Cafe Favorites Turkey Ham & Cheese Deli Flatz Code #C22148/22148
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2386-2016·2016-08-17

    Integra External Fixation System Wire Fixation Bolts Recalled for Breakage

    Integra LifeSciences Corp. is recalling Universal Wire Fixation Bolts because the Slotted Post broke during use at the surgical site.

    Product
    Integra External Fixation System Universal Wire Fixation Bolt - 17.5 mm Catalogue #12224218 ; Integra External Fixation System Universal Wire Fixation Bolt - 23 mm Catalogue #12224219
    Category
    Medical Device
    Distribution
    6 states
  • SevereFDA (Devices)·Z-2402-2016·2016-08-17

    Invacare Bariatric Bed Junction Boxes Recalled for Fire Risk

    Invacare Corporation is recalling 1,011 Bariatric home care beds because the junction boxes may spark, posing a fire hazard in the presence of flammable materials.

    Product
    Junction Boxes, Product Usage: The Invacare Bariatric home care bed is intended to provide a rest surface with adjustable height from floor and adjustable surface contours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2351-2016·2016-08-17

    Richard Allan Scientific Recalls 10% Neutral Buffered Formalin Due to Contamination

    Richard-Allan Scientific Company is recalling 18 cases of 10% Neutral Buffered Formalin due to potential potassium hydroxide contamination that may affect immunohistochemistry test results.

    Product
    Richard Allan Scientific 10% Neutral Buffered Formalin, Part Number: 53901 and 561201 Item 53901 90ml bottle, 125 per case; Item 561201 120ml bottle, 75 per case.
    Category
    Medical Device
    Distribution
    6 states
  • SevereFDA (Devices)·Z-2401-2016·2016-08-17

    Invacare Bariatric Bed Foot Section Recalled for Fire Hazard

    Invacare Corporation is recalling 3,050 Bariatric Bed Foot Sections because a junction box defect may cause sparks and fire.

    Product
    Invacare¿ Foot Section for Semi & Full Electric Beds, Junction Boxes, Product Usage: The Invacare Bariatric home care bed is intended to provide a rest surface with adjustable height from floor and adjustable surface contours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V605000·2016-08-17

    Road Rescue Emergency Vehicles Recalled for Electrical Short Circuit Risk

    REV is recalling 2010-2016 Road Rescue emergency vehicles due to power control modules that may cause short circuits, risking electrical damage, loss of headlights, or fire.

    Product
    ROAD RESCUE — ROAD RESCUE DURAMEDIC, ULTRAMEDIC, TRANSMEDIC, SPECIALTY VEHICLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2399-2016·2016-08-17

    Invacare Bariatric Bed Recalled for Junction Box Fire Risk

    Invacare is recalling 2,184 Bariatric Beds because a defect in the Junction Box may cause sparks, posing a fire hazard in the presence of flammable materials.

    Product
    Invacare¿ Bariatric Bed w/o mattress & rails, Junction Boxes, Product Usage: The Invacare Bariatric home care bed is intended to provide a rest surface with adjustable height from floor and adjustable surface contours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2400-2016·2016-08-17

    Invacare Bariatric Bed Recalled for Potential Fire Hazard from Junction Box Sparks

    Invacare is recalling 2,702 Bariatric Beds because the junction box may spark, posing a fire risk in the presence of flammable materials.

    Product
    Invacare¿ Bariatric Bed with mattress and rails , Junction Boxes, Product Usage: The Invacare Bariatric home care bed is intended to provide a rest surface with adjustable height from floor and adjustable surface contours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2387-2016·2016-08-17

    Integra External Fixation System Slotted Post Recall for Breakage During Use

    Integra LifeSciences is recalling 111 units of External Fixation System Slotted Posts because they broke during use at the surgical site.

    Product
    Integra External Fixation System Slotted Post - Small Catalogue #12224228; Integra External Fixation System Slotted Post Large Catalogue #12224229
    Category
    Medical Device
    Distribution
    6 states
  • SevereNHTSA·16V599000·2016-08-15

    Autocar Recalls 2016-2017 Xspotter Vehicles for Steering Column Defect

    Autocar is recalling 294 model year 2016-2017 Xspotter vehicles because a steering column shaft weld may break, causing a loss of steering ability and increasing crash risk.

    Product
    AUTOCAR — AUTOCAR XSPOTTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V596000·2016-08-12

    Toyota Recalls RAV4 and Lexus HS 250h for Rear Suspension Defect

    Toyota is recalling 2006-2011 RAV4 and 2010 Lexus HS 250h vehicles because improperly tightened rear suspension arms may fail, causing loss of vehicle control.

    Product
    TOYOTA — TOYOTA, LEXUS RAV4, HS 250 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V593000·2016-08-11

    Mazda Recalls CX-7 Vehicles Due to Front Suspension Corrosion Risk

    Mazda is recalling 2007-2012 CX-7 vehicles because water and salt may cause front suspension ball joints to corrode and separate, potentially leading to a loss of steering control.

    Product
    MAZDA — MAZDA CX-7
    Category
    Vehicle
    Distribution
    Distributed nationwide