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.

39576–39600 of 50506

  • HighFDA (Food)·F-1064-2015·2015-02-18

    Damon Industries Recalls Bloody Mary Concentrate Due to Undeclared Anchovies

    Damon Industries is recalling Bloody Mary beverage concentrate because Worcestershire sauce used in the product contains anchovies that were not declared on the label.

    Product
    Fruitful Juice Product Bloody Mary with Tabasco, Beverage Concentrate; Contains 63% Juice; 2 + 1 packed in 2 gal Bag in Box and 3 gallons Bag in Box; UPC - 2 gallon 7 0073 05744 3; UPC - 3 gallon 7 00073 05703 0; Manufactured by Damon Industries, Sparks, NV
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-1097-2015·2015-02-18

    Teleflex Medical Recalls Aquapak 340 SW Humidifier Adaptors Due to Foreign Material

    Teleflex Medical is recalling Aquapak 340 SW humidifier adaptors because packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.

    Product
    AQUAPAK 340 SW, 340 ML W/404 ADAPTOR. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15719·2015-02-18

    Hayneedle Recalls Fiber Optic Christmas Trees Due to Fire Hazard

    Hayneedle is recalling about 220 fiber optic lighted Christmas trees because the motor can overheat and cause a fire. No injuries or property damage have been reported.

    Product
    Artificial Christmas trees
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1065-2015·2015-02-18

    SCC Soft Computer Recalls SoftPath Laboratory Information System Versions

    SCC Soft Computer is recalling specific versions of the SoftPath Laboratory Information System because diagnostic text modifications may not be saved or displayed correctly.

    Product
    SoftPath Laboratory Information System. Versions 4.3.0.8, 4.3.0.9, 4.3.0.10, 4.3.0.11, 4.3.0.12, 4.3.0.14, 4.3.0.15, and 4.4.0.0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V093000·2015-02-18

    Land Rover Recalls Range Rovers Due to Passenger Air Bag Software Issue

    Jaguar Land Rover is recalling 2013-2015 Range Rovers and 2014-2015 Range Rover Sports because the occupant classification system may incorrectly disable the front passenger air bag.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1062-2015·2015-02-18

    Maquet Intra-Aortic Balloon Pump Demonstration Units Recalled for Ferrule Cap Defect

    Maquet Datascope is recalling specific intra-aortic balloon pump demonstration units because a ferrule cap was not removed, which could prevent connection or become dislodged in the device.

    Product
    CARDIOSAVE Intra-Aortic Balloon Pump and CS300 Intra-Aortic Balloon Pump; and, non-sterile, not for human use, SENSATION and SENSATION PLUS IABC demonstration units. Part Number 0998-00-0800-xx; 0998-00-3023-xx; 0998-UC-0800-xx; 0998-UC-3023-xx An electromechanical system…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1041-2015·2015-02-18

    Son In Law BBQ Sauce Recalled for Undeclared Anchovies

    Son In Law Products is recalling Medium Smoking BBQ Sauce and other varieties because they contain anchovies not listed on the label.

    Product
    Medium Smoking BBQ Sauce
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-1082-2015·2015-02-18

    Arrow International Recalls Two-Lumen CVC Kits Due to Foreign Material

    Arrow International Inc is recalling 1,195 ARROWg+ard Blue PLUS Pressure Injectable Two-Lumen CVC Kits because visible foreign material was found inside the kits.

    Product
    ARROWg+ard Blue PLUS Pressure Injectable Two-Lumen CVC Kit. The Multiple-Lumen Catheter permits venous access to the central circulation by way of the femoral jugular, or subclavian veins.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1030-2015·2015-02-18

    MorningStar Farms Chipotle Black Bean Burgers Recalled for Undeclared Peanut

    Kellogg USA Inc is recalling MorningStar Farms Chipotle Black Bean Burgers because they contain undeclared peanut protein.

    Product
    MorningStar Farms Chipotle Black Bean Burger, 38.10 oz (9 ct) - UPC 2898971674; 50.80 oz (12 ct) - UPC 2898940864;
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1201-2015·2015-02-18

    El Campestre Seasoning Mixes Recalled for Undeclared Dyes

    El Campestre, Inc. is recalling Chicken Sasonador, Beef Sasonador, and Adobo Mix due to undeclared Yellow #5 and Yellow #6.

    Product
    El Campestre Adobo Mix Ingredients: Red Chile, Paprika, Water, Vinegar, Orange Juice, Garlic, Salt, & Spices NET WT. 28 LBS. Keep Refrigerated Manufactured by: El Campestre Inc. 1400 S. Santa Fe Avenue Compton, CA 90221 (310) 764-2461
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1027-2015·2015-02-18

    Chicken of the Sea Recalls Chunk Light Tuna Due to Metal Pieces

    Chicken of the Sea is recalling Chunk Light Tuna in Water 12oz cans because they may contain metal pieces from broken equipment.

    Product
    Chicken of the Sea brand Chunk Light Tuna, Case UPC is 4800001164 and the Label UPC is 0 4800001164 0. 100 cases (24 cans/case)
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1063-2015·2015-02-18

    Damon Industries Recalls Bloody Mary Concentrate Due to Undeclared Anchovies

    Damon Industries is recalling Bloody Mary Beverage Concentrate because it contains anchovies that were not declared on the label.

    Product
    Citrus Systems Bloody Mary Beverage Concentrate with Citrus o Flavor; Contains 54% Juice; 2 + 1 packed in 5 gal Bag in Box Manufactured by Damon Industries, Sparks, NV
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-1098-2015·2015-02-18

    Teleflex Medical Recalls Aquapak 340 SW Humidifier Adaptors Due to Foreign Material

    Teleflex Medical is recalling Aquapak 340 SW humidifier adaptors because packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.

    Product
    AQUAPAK 340 SW, 340 ML W/040B ADAPTOR, BRI Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1088-2015·2015-02-18

    Elekta Precise Digital Accelerator Recall for Potential Securing Bolt Failure

    Elekta is recalling 46 Precise Digital Accelerators because securing bolts for the gantry counter frame weight stack may fail.

    Product
    Precise Digital Accelerator Intended to be used for radiation therapy treatments of malignant neoplastic diseases, as determined by a licensed medical practitioner.
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Food)·F-1062-2015·2015-02-18

    Fruitful Juice Bloody Mary Concentrate Recalled for Undeclared Anchovies

    Damon Industries is recalling Fruitful Juice Bloody Mary Beverage Concentrate because it contains anchovies that were not declared on the label.

    Product
    Fruitful Juice Products Bloody Mary Beverage Concentrate with Jalapeno Flavor; Contains 59% Juice; 2 + 1 packed in 3 gal Bag in Box UPC 7 00073 02003 4 Manufactured by Damon Industries, Sparks, NV
    Category
    Food
    Distribution
    5 states
  • HighUSDA FSIS·032-2015·2015-02-17

    Michigan Brand Recalls Pork Sausage for Undeclared Soy Allergen

    Michigan Brand Inc. is recalling pork sausage products because they contain undeclared hydrolyzed soy protein, a known allergen.

    Product
    Michigan Brand Inc. — Michigan Brand, Inc. Recalls Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·15E008000·2015-02-13

    Recaro Bus Driver Seats Recalled for Seat Belt Retraction Defect

    Johnson Controls is recalling Recaro bus driver seats where a tether bar may interfere with the seat belt locking mechanism, increasing injury risk in crashes.

    Product
    SEAT BELTS:FRONT:RETRACTOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E007000·2015-02-13

    Airtex Fuel Pump Modules Recalled Due to Fuel Leak Fire Risk

    Airtex is recalling specific fuel pump modules because an improper seal may cause fuel leaks, increasing the risk of a fire.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1036-2015·2015-02-11

    Invacare Recalls G-Series Bed Rails Due to Entrapment Safety Defect

    Invacare is recalling G-Series bed rails because the mounting bracket does not meet entrapment safety specifications.

    Product
    G- Series Beds; G29 full length bed rails assembly
    Category
    Medical Device
    Distribution
    Distributed nationwide