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.

24751–24775 of 50442

  • HighFDA (Devices)·Z-0066-2020·2019-10-16

    BD FACSLyric Flow Cytometer Recalled for Potential False High Counts

    Becton, Dickinson and Company is recalling 12 BD FACSLyric Flow Cytometers because they may produce falsely high absolute counts when used with specific tubes, potentially affecting clinical decisions.

    Product
    BD FACSLyric Flow Cytometer, 2-Laser 4 Color Instrument, REF: 662875, when using BD Trucount Tubes
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Food)·F-0030-2020·2019-10-16

    Madrona Market Hot Cocoa Mix Recalled for Undeclared Soy

    Diamond Crystal Brands is recalling Madrona Market Hot Cocoa Mix because it contains soy lecithin that is not declared on the label.

    Product
    Madrona Market Delicatessen Hot Cocoa Mix, Net Wt. 2 lb (907 g), Distributed by Food Services of America, Inc. Scottsdale, AZ packaged 6 boxes per case.
    Category
    Food
    Distribution
    18 states
  • HighFDA (Devices)·Z-0067-2020·2019-10-16

    BD FACSLyric Flow Cytometer Recalled for Potential False Absolute Counts

    Becton, Dickinson and Company is recalling specific BD FACSLyric Flow Cytometers used with BD Trucount Tubes due to potential electronic errors that may result in falsely high absolute cell counts.

    Product
    BD FACSLyric Flow Cytometer, 2-Laser 6 Color Instrument, REF: 662876, when using BD Trucount Tubes
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-0079-2020·2019-10-16

    Centurion Medical CVC Bundle Recall Due to Fluid Droplet Risk

    Centurion Medical is recalling CVC bundles containing a recalled BD connector due to potential fluid droplet separation.

    Product
    CVC BUNDLE WITHOUT CATH CVI4600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0080-2020·2019-10-16

    Centurion Medical Recalls Port and IO Access Dressing Kits

    Centurion Medical Products Corporation is recalling Port and IO Access Dressing Kits because they include a connector recalled for potential fluid droplet separation.

    Product
    PORT AND IO ACCESS DRESSING KIT DT15780A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V731000·2019-10-15

    GM Recalls 2020 Cadillac CT6 Vehicles for Tire Pressure Sensor Defect

    General Motors is recalling 2020 Cadillac CT6 vehicles with specific dealer-installed wheels because the tire pressure sensors use the wrong frequency, preventing low-pressure warnings.

    Product
    CADILLAC — CADILLAC CT6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V733000·2019-10-15

    Peterbilt 579 Recall for Incorrect Conspicuity Tape Placement

    PACCAR is recalling 2020 Peterbilt 579 sleeper trucks because conspicuity tape may be installed in the wrong location, reducing visibility to other drivers.

    Product
    PETERBILT — PETERBILT 579
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V730000·2019-10-14

    E-One Recalls Emergency Vehicles Due to Starter Solenoid Circuit Defect

    E-One is recalling specific emergency vehicles because a missing diode in the starter solenoid circuit can damage the lock-out relay, potentially preventing the vehicle from starting.

    Product
    E-ONE — E-ONE TYPHOON, QUEST II, CYCLONE II, CHSH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E069000·2019-10-11

    ASA Electronics Recalls Relay Modules for Voyager Rear Camera Displays

    ASA Electronics is recalling specific relay/capacitor modules used in Voyager rear camera displays. The modules may fail, causing loss of power to the display and increasing crash risk.

    Product
    BACK OVER PREVENTION: SENSING SYSTEM: CAMERA recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V727000·2019-10-11

    Forest River Recalls 2020 Shasta Trailers Due to Axle Hanger Defect

    Forest River is recalling 2020 Shasta Oasis SST30QB and SST31OK trailers because an incorrect axle hanger length may cause the axle to contact the chassis, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER SHASTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V718000·2019-10-10

    2020 Thomas Built Buses Minotour Recall for Seatbelt Warning Light Defect

    Daimler Trucks North America is recalling 2020 Thomas Built Buses Minotour school buses because the seatbelt-unfastened warning light may not illuminate for five seconds after ignition.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0016-2020·2019-10-09

    Valencia Fry Bread Mix Recalled for Undeclared Milk

    Valencia Flour Mill, Ltd. is recalling Valencia Fry Bread Mix because it contains undeclared milk. The product was distributed in New Mexico.

    Product
    Valencia Fry Bread Mix, 2 lbs., packaged in Paper bags with polyliners. UPC 7 30701 33002 4
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0004-2020·2019-10-09

    Metrix Secure EVA Dual Chamber IV Bags Recalled for Leaking

    The Metrix Company is recalling 14,1120 Secure EVA dual chamber IV bags due to a potential for leaking. The affected products were distributed in the US and Canada.

    Product
    SECURE EVA - DUAL CHAMBER CONTAINER with Manifold, 1500mL, REF 66616 (Canadian distribution) - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2257-2019·2019-10-09

    Whole Flower Farms Recalls Chocolate Chip Cookies for Undeclared Soy

    Whole Flower Farms LLC is recalling 27 units of Chocolate Chip Cookies due to undeclared soy lecithin. The product was distributed in Oregon.

    Product
    Chocolate Chip Cookie, net wt. 2 oz. The product was distributed frozen and has a 5-day shelf life after being defrosted at the stores. The label is read in parts: "***Chocolate Chip Cookie*** Ingredients: Sunflower oil, brown sugar, almond milk, evaporated cane juice…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0019-2020·2019-10-09

    Paltop Advanced Plus Dental Implant Recall for Surface Topography Defects

    Paltop Advanced Dental Solutions is recalling 167 dental implants because surface micro/nano topography may be inconsistent. The recall covers units distributed to 16 states.

    Product
    Paltop Advanced Plus Dental Implant Dia 6.0mm L10mm Catalog Number: 20-70024P
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Drugs)·D-0056-2020·2019-10-09

    KRS Global Biotechnology Recalls Human Chorionic Gonadotropin Due to Sterility Concerns

    KRS Global Biotechnology is recalling 6,620 vials of Human Chorionic Gonadotropin 11,000 Units due to a lack of assurance of sterility.

    Product
    Human Chorionic Gonadotropin 11,000 Units/Vials Lyophilized For SC/IM Use, Rx Only, KRS Global Biotechnology 791 Park of Commerce Blvd, Boca Raton, FL 33487. NDC 3321673974
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2760-2019·2019-10-09

    Howmedica Recalls Triathlon Femoral Distal Augments Due to Device Overhang

    Howmedica Osteonics Corp. is recalling 159 units of Triathlon Femoral Distal Augments because a device overhang protrudes beyond the mating femoral component.

    Product
    TRIATHLON FEMORAL DISTAL AUGMENT 15MM - SIZE 2 RIGHT Catalog # 5542-A-202 - Product Usage: Triathlon Femoral Distal Augments are used with Triathlon TS Femoral Components during revision Total Knee Arthroplasty (TKA) and with Triathlon Primary PS Femoral Components during TKA…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V717000·2019-10-09

    2020 Thomas Built Buses Minotour Recalled for Seatbelt Warning Light Defect

    Daimler Trucks North America is recalling 2020 Thomas Built Buses Minotour school buses because the seatbelt-unfastened warning light may not illuminate for five seconds after ignition.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0024-2020·2019-10-09

    Stryker C2 Nerve Monitor Recalled for Potential Nerve Injury Risk

    Stryker is recalling 135 C2 Nerve Monitor units because design and instruction issues may lead to use errors that cause nerve injury.

    Product
    C2 Nerve Monitor, 8 Channel, 5140-508-280, UDI 07613327277319 Product Usage: The C2 Nerve Monitor System is intended for intra-operative monitoring and stimulation for localization and identification of cranial and peripheral motor and mixed motor sensory nerves during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0023-2020·2019-10-09

    Stryker Recalls C2 Nerve Monitor Due to Usability Design Issues

    Stryker is recalling 135 C2 Nerve Monitor units because design and instruction usability issues may lead to use errors and potential nerve injury.

    Product
    C2 Nerve Monitor, 4 Channel, 5140-508-240, UDI 07613327177329 Product Usage: The C2 Nerve Monitor System is intended for intra-operative monitoring and stimulation for localization and identification of cranial and peripheral motor and mixed motor sensory nerves during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2256-2019·2019-10-09

    Whole Flower Farms Peanut Butter Chocolate Chip Cookies Recalled for Undeclared Soy

    Whole Flower Farms LLC is recalling Peanut Butter Chocolate Chip Cookies due to undeclared soy lecithin. The product was distributed in Oregon.

    Product
    Peanut Butter Chocolate Chip Cookie, net wt. 2 oz. The product was distributed frozen and has a 5-day shelf life after being defrosted at the stores. The label is read in parts: "***Peanut Butter Chocolate Chip Cookie*** Ingredients: Peanut Butter, evaporated cane juice…
    Category
    Food
    Distribution
    1 state