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.

21451–21475 of 32121

  • SevereNHTSA·15V754000·2015-11-13

    Daimler Recalls 2016 Minotour School Buses for Wiring Fire Risk

    Daimler Trucks North America is recalling 27 model year 2016 Minotour school buses because an incorrectly routed wiring harness may cause a loose power cable, increasing the risk of an electrical arc and fire.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16708·2015-11-12

    WakaWaka Recalls Electrical Adapter Kits Due to Fire and Shock Hazards

    WakaWaka is recalling electrical adapter kits because they can overheat, smoke, or explode, posing risks of fire and electrical shock. No injuries have been reported.

    Product
    Electrical adapter kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V748000·2015-11-12

    Goshen Coach Recalls Buses with Defective Ricon Wheelchair Lifts

    Goshen Coach is recalling 2006-2015 buses equipped with certain Ricon wheelchair lifts due to a defect that could cause the platform to fall out of the vehicle.

    Product
    GOSHEN — GOSHEN G-FORCE, SENTINEL UC, SENTINEL, PACER LTD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0223-2016·2015-11-11

    Bard Flair Endovascular Stent Graft Recalled for Deployment Failures

    Bard Peripheral Vascular is recalling 292 units of the FLAIR Endovascular Stent Graft due to potential deployment failures during use.

    Product
    FLAIR Endovascular Stent Graft, Product Code: FAS08070, FAF08070, Implant Size: 8mmx70mm The FLAIR Endovascular Stent Graft (implant) is a flexible, self-expanding endoprosthesis comprised of expanded polytetrafluoroethylene (ePTFE) encapsulating a Nitinol stent framework. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0137-2016·2015-11-11

    Biscomerica Recalls Cocoa Buttons for Undeclared Milk Allergen

    Biscomerica, Inc. is recalling specific lots of cocoa buttons because they contain undeclared milk. The product was distributed in Ohio.

    Product
    Cocoa buttons, item no. 80203, 80203-1, 25lb bulk case
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0131-2016·2015-11-11

    Shearer's Foods Recalls On The Border Tortilla Chips for Milk Exposure

    Shearer's Foods is recalling On The Border Cafe Style Tortilla Chips because they may have been exposed to a milk-containing ingredient.

    Product
    ON THE BORDER MEXICAN GRILL & CANTINA Cafe Style Tortilla Chips 18 oz. bags
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-0132-2016·2015-11-11

    Nijay International Recalls Organic Coriander Powder for Salmonella Risk

    Nijay International is recalling specific lots of Organic Coriander Powder due to potential Salmonella contamination. The product was distributed in Texas.

    Product
    Organic Coriander Powder (Dhania Powder), 60packs/case, UPC 40074 13813
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0129-2016·2015-11-11

    MBG Marketing Recalls Naturipe Frozen Blueberries Due to Salmonella Risk

    MBG Marketing is recalling select pallets of Naturipe IQF Blueberries due to the potential presence of Salmonella.

    Product
    Naturipe Foods Frozen Blueberries, IQF, 30 lb. boxes and 1500 lb. Totes, packed in cardboard boxes with plastic bag liners; 50 boxes per pallet or 1 Tote per pallet
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0123-2016·2015-11-11

    Evolution Fresh Greek Yogurt Recalled for Undeclared Almonds

    Greencore USA is recalling Evolution Fresh Nonfat Greek Yogurt with Strawberry and Granola because it may contain undeclared almonds.

    Product
    Evolution Fresh Nonfat Greek Yogurt with Strawberry and Granola, 6.1oz., UPC: 7 6211107474 4
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-0149-2016·2015-11-11

    Earth Exotic Brussels Sprouts Recalled for Potential Listeria Contamination

    A.M.S. Exotic LLC is recalling Earth Exotic Brussels Sprouts due to potential Listeria monocytogenes contamination. The product was distributed in Connecticut and South Carolina.

    Product
    Earth Exotic Brussels Sprouts Net. Wt. 8 oz. (227 g) Net. Wt. 32 oz (2 LBS) 907 g
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0136-2016·2015-11-11

    Del Monte Recalls Granny Smith Apples Due to Listeria Risk

    Del Monte Fresh Produce is recalling 5,962 Granny Smith apples in eight states due to potential Listeria monocytogenes contamination.

    Product
    Granny Smith green apples, shipped in unmarked plastic bags and cardboard boxes. Sold individually in retail stores.
    Category
    Food
    Distribution
    9 states
  • SevereNHTSA·15V743000·2015-11-10

    Van Hool Recalls 2015-2016 Motorcoaches Due to Air Brake Defect

    Van Hool is recalling 48 model year 2015-2016 TD925 and TDX25 motorcoaches because air brakes may take too long to release, potentially causing brake drag, heat buildup, or fire.

    Product
    VAN HOOL — VAN HOOL TD925, TDX25
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V744000·2015-11-10

    Maserati Recalls 2016 GranTurismo Vehicles Due to Door Latch Defect

    Maserati is recalling 135 model year 2016 GranTurismo vehicles because passenger side door latches may not be heat treated, increasing injury risk in a crash.

    Product
    MASERATI — MASERATI GRANTURISMO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V746000·2015-11-10

    Spartan MetroStar and Defense Chassis Cabs Recalled for Axle Nut Issue

    Spartan Motors is recalling 2014-2015 MetroStar and Defense Department chassis cabs because improperly tightened axle nuts may cause the driveshaft to disconnect.

    Product
    SPARTAN — SPARTAN METROSTAR, DEFENSE DEPT. CHASSIS CAB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V740000·2015-11-09

    Peterbilt Auto Haulers Recalled for Tire Speed Rating Mismatch

    PACCAR is recalling specific Peterbilt auto haulers because front tires have a lower speed rating than the vehicle's maximum speed, increasing crash risk.

    Product
    PETERBILT — PETERBILT 386, 348, 340, 337
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V739000·2015-11-09

    BMW Recalls 2014-2015 MINI Cooper Vehicles for Airbag Calibration Issue

    BMW is recalling 2014-2015 MINI Cooper and Cooper S vehicles because incorrectly calibrated seat sensors may cause inappropriate airbag activation or deactivation during a crash.

    Product
    MINI — MINI COOPER, COOPER S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·139-2015·2015-11-07

    Cloverdale Foods Recalls Beef and Pork Bratwurst for Undeclared Milk Allergen

    Cloverdale Foods is recalling beef and pork bratwurst mislabeled as beef frankfurters because it contains undeclared milk, a known allergen.

    Product
    Cloverdale Foods Co. — Cloverdale Foods Company Recalls Beef and Pork Product Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·140-2015·2015-11-07

    Boulder Natural Meats Recalls Beef, Pork, and Poultry for Undeclared Allergen

    Boulder Natural Meats is recalling approximately 3,607 pounds of beef, pork, and poultry products due to misbranding and undeclared milk allergen.

    Product
    Boulder Natural Meats Recalls Beef, Pork, and Poultry Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    3 states
  • SevereUSDA FSIS·138-2015·2015-11-06

    Maple Leaf Foods Recalls Boneless Pork Shoulders for Import Inspection Violation

    Maple Leaf Foods is recalling approximately 4,030 pounds of boneless pork shoulders that entered the U.S. without inspection. The products were shipped to retail locations in California.

    Product
    Maple Leaf Foods Inc. Recalls Boneless Pork Products Produced Without Benefit of Import Inspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·15V737000·2015-11-06

    Outdoors RV Recalls Trailers Due to Fire Risk from Pinched Wires

    Outdoors RV is recalling 2015-2016 Timber Ridge, Glacier Peak, Wind River, and Black Stone trailers because liquid propane hoses and electrical wires may be pinched or scraped, increasing the risk of fire.

    Product
    OUTDOORS RV — OUTDOORS RV TIMBER RIDGE, GLACIER PEAK, WIND RIVER, BLACK STONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V733000·2015-11-05

    Nissan Recalls 2015 Altima and 2016 Maxima for Brake Caliper Bolt Issue

    Nissan is recalling specific 2015 Altima and 2016 Maxima vehicles because front brake caliper mounting bolts may not be properly tightened, which could reduce braking ability.

    Product
    NISSAN — NISSAN ALTIMA, MAXIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0144-2016·2015-11-04

    Moses Lake Pharmacy Recalls Testosterone Propionate Injectable Solution

    JD & SN Inc. is recalling 5 syringes of Testosterone Propionate Injectable Solution due to a lack of assurance of sterility.

    Product
    TESTOSTERONE PROPRIONATE, Injectable Solution, 100 mg/mL, syringe size: 10mL, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0080-2016·2015-11-04

    FDA Recalls Estradiol Pellets Due to Sterility Assurance Concerns

    JD & SN Inc. is recalling Estradiol 18 mg pellets because the company cannot assure the sterility of the product. The recall covers all sterile human compounded drugs within their expiry date.

    Product
    ESTRADIOL, Pellet, 18 mg, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
    Category
    Drug
    Distribution
    Distributed nationwide