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.

11951–11975 of 29163

  • SevereFDA (Devices)·Z-1734-2019·2019-06-12

    Getinge Meera Mobile Operating Table Recalled for Electric Shock Risk

    Maquet Cardiovascular is recalling Getinge Meera Mobile Operating Tables because exposed electronic components may cause electric shock to users.

    Product
    GETINGE MEERA MOBILE OPERATING TABLE: (1) Part 720001B2 (2) Part 720001B0 (3) Part 720001F2 (4) Part 720001F0 (5) Part 710001B2 (6) Part 710001B0 (7) Part 710001F0 Product Usage: The Meera Mobile Operating Table is designed to support and position the patient…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V446000·2019-06-12

    Porsche Recalls Vehicles Due to Gear Selector Bushing Defect

    Porsche is recalling specific Cayenne and Panamera models because a degraded bushing may allow the driver to exit the vehicle while the transmission is not in Park, increasing crash risk.

    Product
    PORSCHE — PORSCHE PANAMERA, CAYENNE S, CAYENNE TURBO, CAYENNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1231-2019·2019-06-12

    OriGen ECMO Reinforced Dual Lumen Cannula Recalled for Adhesive Failure Risk

    OriGen Biomedical is recalling 61 units of ECMO Reinforced Dual Lumen Cannulas due to a risk of tube disconnection from the hub caused by adhesive failure.

    Product
    ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV19F
    Category
    Medical Device
    Distribution
    33 states
  • SevereFDA (Food)·F-1433-2019·2019-06-12

    Topnotch Foods Natural Bread Crumbs Recalled for Undeclared Milk

    Topnotch Foods Inc is recalling 2,000 lbs of Natural Bread Crumbs due to undeclared milk. The product was distributed in California.

    Product
    Topnotch Foods Natural Bread Crumbs: 50 lb. Net Wt. 22.68 kg. and 10 lbs. 4.54 Kg. Item number 10021: Vernon, CA Correct Ingredients: Enriched, Bleached & Unbleached, Wheat Flour, [Flour, Malted Barley Flour, Niacin, Reduced Iron, Thiamine Mononitrate, Riboflavin…
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·19V443000·2019-06-11

    Freightliner M2 and 108SD Trucks Recalled for Axle Lubrication Defect

    Daimler Trucks North America is recalling 2019-2020 Freightliner M2 and 2020 108SD trucks because insufficient axle lubrication may damage wheel bearings, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V444000·2019-06-11

    Thomas Built Buses Recall School Buses Due to Dragging Rear Brakes

    Daimler Trucks North America is recalling specific Thomas Built Buses school buses because the driver-side rear brakes may drag, increasing the risk of smoke and fire.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, SAF-T-LINER HDX, SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V433000·2019-06-10

    Ford Recalls 2013 F-150s for Transmission Downshifting Risk

    Ford is recalling 2013 F-150 trucks with 5.0L or 6.2L engines previously repaired under recall 19V-075 because the transmission may unexpectedly downshift into first gear, increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V432000·2019-06-10

    Ford Recalls Econoline Vehicles Due to Transmission Weld Failure Risk

    Ford is recalling 2009-2016 Econoline vehicles with specific transmissions and emergency packages due to a weld defect that may cause sudden loss of drive power.

    Product
    FORD — FORD ECONOLINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V431000·2019-06-08

    Farber Specialty Vehicles Recalls 2018 XCR Models Due to Brake Bolt Issue

    Farber Specialty Vehicles is recalling 2018 XCR specialty vehicles because brake caliper mounting bolts may not be sufficiently tightened, which can reduce brake effectiveness and increase crash risk.

    Product
    FCCC — FCCC XCR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V425000·2019-06-07

    Mazda Recalls 2019 Mazda3 Vehicles Due to Loose Lug Nuts

    Mazda is recalling 2019 Mazda3 vehicles because lug nuts may loosen, potentially causing a wheel to detach and increasing crash risk.

    Product
    MAZDA — MAZDA MAZDA3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·066-2019·2019-06-07

    Tyson Recalls Chicken Fritters Due to Possible Hard Plastic Contamination

    Tyson Foods is recalling approximately 190,757 pounds of ready-to-eat chicken fritters that may contain hard plastic. The products were shipped to institutional foodservice locations nationwide.

    Product
    Tyson Foods, Inc. — Tyson Foods, Inc. Recalls Ready-To-Eat Chicken Fritter Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·065-2019·2019-06-06

    Table 87 Frozen Recalls Pork Pizza Produced Without Federal Inspection

    Table 87 Frozen, LLC is recalling approximately 649 pounds of frozen prosciutto pizzas produced without federal inspection. No adverse reactions have been reported.

    Product
    Table 87 Frozen, LLC — Table 87 Frozen, LLC Recalls Pork Pizza Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V424000·2019-06-06

    Acura Recalls 2016-2019 ILX Vehicles for Driveshaft Separation Risk

    Acura is recalling 2016-2019 ILX vehicles because excessive grease may prevent a set-ring from engaging, allowing the driveshaft to separate and increase crash risk.

    Product
    ACURA — ACURA ILX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V422000·2019-06-06

    2020 International HV Trucks Recalled for Wheel Bearing Lubrication Defect

    Navistar is recalling 2020 International HV Severe Service Diesel Trucks because insufficient steer axle hub lubrication may cause wheel bearing damage and potential wheel separation.

    Product
    INTERNATIONAL — INTERNATIONAL HV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1573-2019·2019-06-05

    Maquet Getinge Adult ECC Pack Recall Due to Sterility Assurance Concerns

    Maquet Cardiovascular is recalling Adult ECC Packs because a design feature may prevent sterilization gas from reaching all fluid paths, potentially compromising sterility.

    Product
    Maquet Getinge-BO-TOP 36504 ADULT ECC PACK Material: 701065765
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1519-2019·2019-06-05

    Maquet Custom Tubing Sets Recalled Due to Sterility Assurance Concerns

    Maquet Cardiovascular is recalling custom tubing sets for extracorporeal circulation because a design feature may prevent sterilization gas from reaching all fluid paths.

    Product
    Maquet Getinge-BEQ-TOP 27901 SMALL PATIENT CI Material:701052287
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1526-2019·2019-06-05

    Maquet Getinge Custom Tubing Sets Recalled for Sterility Assurance Concerns

    Maquet Cardiovascular is recalling specific custom tubing sets for extracorporeal circulation because a design flaw may prevent proper sterilization of the stopcock ports.

    Product
    Maquet Getinge-BO-TOP 20705 SMALL PATIENT 1/4 Material: 701053486
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1537-2019·2019-06-05

    Maquet Getinge ECC Tubing Sets Recalled for Sterility Assurance Concerns

    Maquet Cardiovascular is recalling specific ECC tubing sets because a design feature may prevent proper sterilization, potentially compromising sterility.

    Product
    Maquet Getinge-BEQ-T 8025 1/4" ECC Pack with RF32 Material:701055142
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1547-2019·2019-06-05

    Maquet Getinge ECC Tubing Sets Recalled Due to Sterility Assurance Concerns

    Maquet Cardiovascular is recalling specific batches of Getinge-BEQ-TOP 38900 ECC Packs because a design flaw may prevent proper sterilization of the stopcock ports.

    Product
    Maquet Getinge-BEQ-TOP 38900 ECC PACK Material: 701056368
    Category
    Medical Device
    Distribution
    Distributed nationwide