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.

43926–43950 of 50511

  • HighFDA (Food)·F-1106-2013·2013-03-20

    Dakota Specialty Milling Recalls Multigrain Mix for Metal Wire Mesh Contamination

    Dakota Specialty Milling is recalling specific lots of multigrain mix due to potential contamination with pliable metal wire mesh fragments from a defective sifter.

    Product
    42204, MULTIGRAIN MIX FOR P.S. BREAD ( WHITE WHEAT, OATS, BARLEY, TRICALE, BROWN FLAX, CORN, SESAME SEED, POTATO FLAKES, WHEAT, RYE, WHEAT BRAN), DAKOTA SPECIALTY MILLING, INC., FARGO, ND , 1 NET WT. 50 LBS .
    Category
    Food
    Distribution
    21 states
  • HighNHTSA·13V100000·2013-03-19

    Starcraft XLT Buses Recalled for Incorrect Weight Rating Labels

    Starcraft Bus is recalling 2004-2009 XLT buses because incorrect weight rating labels could lead to improper loading and tire failure.

    Product
    STARCRAFT — STARCRAFT XLT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V097000·2013-03-15

    GM Recalls 2013 Buick LaCrosse and Cadillac SRX for Transmission Software Issue

    General Motors is recalling 2013 Buick LaCrosse and Cadillac SRX vehicles because a software defect may cause the transmission to shift to Sport mode, removing engine braking and increasing crash risk.

    Product
    BUICK — BUICK, CADILLAC LACROSSE, SRX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V098000·2013-03-15

    Toyota Recalls FJ Cruiser Models Due to Seat Belt Anchor Defect

    Toyota is recalling 2007-2013 FJ Cruisers because cracks in the rear door panel may cause the front seat belt retractors to detach, increasing injury risk in a crash.

    Product
    TOYOTA — TOYOTA FJ CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V093000·2013-03-15

    Acura TSX vehicles are recalled due to engine-stall risk

    Honda is recalling certain 2004-2008 Acura TSX vehicles sold in or registered in specified states. Corrosion can damage the engine control unit and potentially cause the engine to stall, increasing crash risk.

    Product
    ACURA — ACURA TSX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V094000·2013-03-14

    Nissan Recalls 2013 Titan and NV Trucks for Shift Lever Defect

    Nissan is recalling 2013 Titan trucks and NV vans because a shift lever defect may allow the vehicle to roll away without the brake being applied.

    Product
    NISSAN — NISSAN TITAN, NV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1057-2013·2013-03-13

    R-Kane Z Pro High Protein Supplement Recalled for Undeclared Allergens

    R-Kane Products Inc. is recalling Z Pro 25 High Protein Supplement because the individual packets contain undeclared milk and soy allergens.

    Product
    Z Pro 25 High Protein Supplement Net. Wt. 1.5 oz. - Chocolate Flavor Formulated and Distributed by: R-Kane Products, Inc. 8351 National Highway, Pennsauken, NJ 08110
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0907-2013·2013-03-13

    Siemens ARTISTE syngo RT Therapist software recall for beam delivery error

    Siemens is recalling 5 ARTISTE digital linear accelerators due to a software defect that may cause repeated delivery of radiation beams.

    Product
    SIEMENS brand ARTISTE syngo RT Therapist (RTT) version 4.3, ARTISTE Model, Part No. 08162815, Digital linear accelerators, MOSAIQ OIS system, Distributed by SIEMENS Healthcare IM CR RO, CR Radiation Oncology, Manufactured by SIEMENS AG, MEDICAL SOLUTIONS, GERMANY.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1051-2013·2013-03-13

    Deep Foods Recalls Dry Garlic Chutney for Unapproved Dye

    Deep Foods Inc. is recalling 4-ounce jars of Dry Garlic Chutney because the product contains unapproved dyes, Rhodamine B and Basic Violet 10.

    Product
    Deep Best Quality Dry Garlic Chutney (Thechaa); Net Wt. 4 OZ.; UPC 011433111201; Deep Foods, Inc. Union, NJ 07083
    Category
    Food
    Distribution
    27 states
  • HighFDA (Devices)·Z-0901-2013·2013-03-13

    GE Healthcare Recalls Advantage Workstation Volume Viewer Software

    GE Healthcare is recalling Advantage Workstation Volume Viewer software due to potential safety issues that may result in incorrect views and measurements.

    Product
    GE Healthcare Volume Viewer Plus 5.x (Advantage Workstation 4.2) Volume Viewer 3.x (Advantage Workstation 4.1) Volume Analysis (Advantage Workstation 4.0) Volume Analysis (Advantage Workstation 3.1) Advantage Windows Volume Rendering Option is intended to provide fast…
    Category
    Medical Device
    Distribution
    27 states
  • HighFDA (Devices)·Z-0908-2013·2013-03-13

    Medtronic DPL Single Stage Venous Cannula Recalled for Rough Metal Edges

    Medtronic is recalling DPL Single Stage Venous Cannulas used in cardiopulmonary bypass due to potential rough metal edges on the tip side ports.

    Product
    Medtronic DPL Single Stage Venous Cannula with Metal Tip, used in cardiopulmonary bypass procedures. Model numbers: 67312; 67314; CB67314; 67316; 67318; CB67318; 67320; 69312; 69314; 69316; 69318; 69320; 69322; 69324; 69328; 69331.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1056-2013·2013-03-13

    Z Pro 25 High Protein Supplement Recalled for Undeclared Allergens

    R-Kane Products Inc. is recalling Z Pro 25 High Protein Supplement because it contains undeclared milk and coconut allergens.

    Product
    Z Pro 25 High Protein Supplement Net. Wt. 1.3 oz. - Vanilla Flavor Formulated and Distributed by: R-Kane Products, Inc. 8351 National Highway, Pennsauken, NJ 08110
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0918-2013·2013-03-13

    Ethicon PSX PROXIMATE Skin Staple Extractor Recalled for Sterility Concerns

    Ethicon Endo-Surgery is recalling PSX PROXIMATE Skin Staple Extractors because packaging damage may have compromised the sterility of the devices.

    Product
    PSX PROXIMATE Skin Staple Extractor, ETHICON ENDO-SURGERY, LLC. For routine skin closure in a wide variety of surgical procedures.
    Category
    Medical Device
    Distribution
    49 states
  • HighFDA (Food)·F-1054-2013·2013-03-13

    Rich Products Recalls Daphne's Multigrain Flatbread Due to Metal Fragments

    Rich Products Corp is recalling Daphne's California 6 inch Multigrain Flatbread because the bulk flour used contained stainless steel fragments.

    Product
    Daphne's California 6 inch Multigrain Flatbread, 2.1 oz., Product Code 77468, Net Wt. 13.50 lbs. (case) --- There are 12 - 10 count bags per case
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-0906-2013·2013-03-13

    Philips CT System Software Recall for Incorrect Value Display

    Philips is recalling 2,580 Extended Brilliance Workspace CT systems to fix a software defect that may display incorrect values.

    Product
    Philips Medical System Extended Brilliance Workspace (EBW), Computed Tomography X-Ray System. The Extended Brilliance Workspace (EBW) is a component of the Computed Tomography X-Ray System that is intended to produce cross-sectional images of the body by computer…
    Category
    Medical Device
    Distribution
    38 states
  • HighNHTSA·13V072000·2013-03-12

    Caterpillar Recalls CT660 Trucks for Missing Side Marker Lamps

    Caterpillar is recalling 2012 and 2014 CT660 heavy-duty trucks because missing side marker lamps or reflective tape reduce visibility and increase crash risk.

    Product
    CATERPILLAR — CATERPILLAR CT660
    Category
    Vehicle
    Distribution
    Distributed nationwide