The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

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.

32026–32050 of 50502

  • HighFDA (Devices)·Z-2546-2017·2017-06-21

    Medtronic Recalls USPACK Suture Kits Due to Potential Seal Defects

    Medtronic is recalling USPACK-SUTURE KITs (Item US1672) because an incomplete inner package seal may cause the suture material to degrade prematurely.

    Product
    USPACK-SUTURE KIT; Item Number: US1672
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2358-2017·2017-06-21

    Bright Farms Spinach Blend Recalled Due to Metal Contamination

    Bright Farms is recalling Spinach Blend (4 oz. packages) because metal was detected in the product. The firm identified the issue through internal verification techniques.

    Product
    Bright Farms Spinach Blend (4 oz. package) , The salad products packaged in clear, plastic clamshells with best by dates on the package .
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-2382-2017·2017-06-21

    Biomerieux Recalls VITEK 2 Gram Negative Susceptibility Cards Due to Moisture Risk

    Biomerieux Inc is recalling VITEK 2 Gram Negative Susceptibility cards because compromised container integrity may expose the product to moisture, potentially causing antibiotic degradation.

    Product
    VITEK¿ 2 Gram Negative Susceptibility card (AST-N190), REF 412548, 20 cards per carton.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2405-2017·2017-06-21

    Biomerieux Recalls VITEK 2 Gram Negative Susceptibility Cards

    Biomerieux Inc is recalling VITEK 2 Gram Negative Susceptibility cards because container integrity may be compromised, exposing the product to moisture and causing antibiotic degradation.

    Product
    VITEK¿ 2 Gram Negative Susceptibility card (AST-N227), REF 413144, 20 cards per carton.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·17751·2017-06-20

    Kawasaki Recalls Utility and Off-Highway Vehicles Due to Fire Hazard

    Kawasaki is recalling approximately 6,600 utility, recreational off-highway, and all-terrain vehicles because a fuel gauge retainer can collapse and leak fuel, posing a fire hazard.

    Product
    Utility vehicles, recreational off-highway vehicles and all-terrain vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17180·2017-06-20

    Staples Recalls Hazen Mesh Task Chairs Due to Fall Hazard

    Staples is recalling Hazen Mesh Task chairs because the legs can break, posing a fall hazard. Consumers should stop using the chairs and contact Staples for a free replacement base.

    Product
    Hazen Mesh Task chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V386000·2017-06-19

    BYD Recalls 2015-2016 K7 M Buses for Wiper Arm Defect

    BYD is recalling 2015-2016 K7 M buses because wiper arms may crack and detach, reducing visibility and increasing crash risk.

    Product
    BYD — BYD K7 M
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V385000·2017-06-19

    Starcraft RV Recalls 2018 Launch Outfitter Trailers for Electrical Outlet Defect

    Starcraft RV is recalling 2018 Launch Outfitter travel trailers because an electrical outlet lacks Ground Fault Circuit Interrupter protection, increasing the risk of electrical shock.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT LAUNCH OUTFITTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17750·2017-06-16

    Advanced Composites Recalls Bicycle Forks Due to Fall Hazard

    Advanced Composites is recalling about 40 Wound Up Tandem Duo Disc bicycle forks because the fork leg can crack, posing a fall hazard.

    Product
    Bicycle forks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V382000·2017-06-15

    GM Recalls 2014-2016 Chevrolet SS Vehicles for Steering Defect

    General Motors is recalling 2014-2016 Chevrolet SS vehicles because corrosion may cause a loss of electric power steering assist, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET CHEVEROLET SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2328-2017·2017-06-14

    Parade Deli Cake Recalled for Undeclared Soy Lecithin

    Choice Northwest is recalling Paradise Deli brand Love Your Heart Cake because it contains undeclared soy lecithin. The product was distributed in Oregon.

    Product
    Love Your Heart Cake, Paradise Deli brand, Net Wt. 14 oz., UPC 0 31619 40402 6. The label is read in parts: "***Contains: Fresh apples, fresh carrots, organic unbleached wheat flour, organic cane sugar, Oregon grown hazelnuts, raisins, cinnamon, baking soad, and baking…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2233-2017·2017-06-14

    ConvaTec Recalls Non-Rebreather Oxygen Masks Due to Quality Concerns

    ConvaTec, Inc. is voluntarily recalling specific lots of Non-Rebreather Oxygen Masks. The recall was initiated due to quality concerns, though no specific defect is described in the source.

    Product
    Non-Rebreather Oxygen Mask, Adult High Concentration with 2.1 m (7) Oxygen Tubing, Product Code 108MM
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Food)·F-2354-2017·2017-06-14

    Alaska Pasta Company Recalls Refrigerated Shells for Undeclared Soy Lecithin

    Alaska Pasta Company is recalling 52.50 lbs of refrigerated shells due to undeclared soy lecithin from cooking spray. The product was distributed in Alaska.

    Product
    Shells. Product is made refrigerated. Product is packaged in plastic containers. The plastic containers are marked on the side of the container with the customer name (middle top), date of production (bottom left), and weight of product in lbs (bottom right). Some containers…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-2317-2017·2017-06-14

    Aunt Jemima Cinnamon Swirl French Toast Recalled for Listeria Risk

    Pinnacle Foods is recalling Aunt Jemima Cinnamon Swirl Thick French Toast nationwide due to potential Listeria monocytogenes contamination.

    Product
    Aunt Jemima(R) Cinnamon Swirl Thick French Toast, 144 COUNT, NET WT 10.7 LBS, UPC 001960043584
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2234-2017·2017-06-14

    ConvaTec Recalls Non-Rebreather Masks Due to Potential Valve Defect

    ConvaTec, Inc. is voluntarily recalling specific lots of Non-Rebreather Masks due to a potential defect in the check valve. The recall covers units distributed in the US and internationally.

    Product
    Non-Rebreather Mask, Reservoir Bag, Check Valve, Two Side Valves, No Tubing, Product Code 226MM
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Food)·F-2353-2017·2017-06-14

    Alaska Pasta Company Recalls Refrigerated Rigatoni for Undeclared Soy Lecithin

    Alaska Pasta Company is recalling 67.50 lbs of refrigerated rigatoni because it contains undeclared soy lecithin from cooking spray. The product was distributed only in Alaska.

    Product
    Riggatoni. Product is made refrigerated. Product is packaged in plastic containers. The plastic containers are marked on the side of the container with the customer name (middle top), date of production (bottom left), and weight of product in lbs (bottom right). Some…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-2300-2017·2017-06-14

    Aunt Jemima Homestyle French Toast Recalled for Listeria Risk

    Pinnacle Foods is recalling Aunt Jemima Homestyle French Toast due to potential Listeria monocytogenes contamination.

    Product
    AUNT JEMIMA(R) HOMESTYLE FRENCH TOAST, 6 COUNT, NET WT 12.5oz, UPC 019600057703
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2308-2017·2017-06-14

    Arrow International Recalls Hemodialysis Catheterization Kits

    Arrow International Inc. is recalling ARROWg+ard Blue You-Bend Two-Lumen Hemodialysis Catheterization Kits due to a Class II recall.

    Product
    ARROWg+ard Blue You-Bend Two-Lumen Hemodialysis Catheterization Kit for High Volume Infusions The Arrow(r) CVC is indicated to provide short-term ( < 30 days) central venous access for treatment of diseases or conditions requiring central venous access including, but not…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2315-2017·2017-06-14

    Aunt Jemima Whole Grain Mini Pancakes Recalled for Listeria Risk

    Pinnacle Foods is recalling Aunt Jemima Whole Grain Mini Pancakes due to a potential for Listeria monocytogenes contamination.

    Product
    Aunt Jemima(R) Whole Grain Mini Pancakes, 12-40 COUNT, NET WT 12 LBS, UPC 001960043558
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2314-2017·2017-06-14

    Aunt Jemima Cinnamon Swirl French Toast Recalled for Listeria Risk

    Pinnacle Foods is recalling Aunt Jemima Cinnamon Swirl French Toast due to potential Listeria monocytogenes contamination.

    Product
    Aunt Jemima(R) Cinnamon Swirl French Toast, 144 COUNT, NET WT 13.5 LBS, UPC001960005880
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2228-2017·2017-06-14

    ConvaTec Recalls Elongated Oxygen Masks Due to Tubing Detachment Risk

    ConvaTec is recalling elongated oxygen masks because tubing may detach from the connector, potentially disrupting oxygen supply to users.

    Product
    Oxygen Masks, Elongated (under chin), Adult Med Conc., No Tubing, Product Code 104-E;
    Category
    Medical Device
    Distribution
    14 states