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.

39526–39550 of 50506

  • HighFDA (Food)·F-1213-2015·2015-02-25

    My Sweet Ol' Etcetera Recalls Peanut Butter Brownies for Undeclared Soy

    My Sweet Ol' Etcetera is recalling 36 units of Peanut Butter Brownies distributed in Oregon due to undeclared soy lecithin.

    Product
    Peanut Butter Brownie, refrigerated, single slice wrapped in cellophane, net wt. 8 oz. The product's label read in parts: "***New item My sweet ol' etcetera bakery***Peanut Butter brownie, org wheat flour, org. egg, butter, vanilla, sugar, unsw chocolate, Buttercream natural…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1205-2015·2015-02-25

    Condies Foods Recalls Salsas Due to Undeclared Peanut Allergen

    Condies Foods is recalling specific salsa products because they contain cumin that may have undeclared peanut protein.

    Product
    Dr. J's Smart Gourmet SalsaMedium, 15 oz., UPC: 793573939166 (Medium).
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1116-2015·2015-02-25

    Terumo HX2 Temperature Management System Recalled for Valve Malfunction

    Terumo is recalling 103 HX2 Temperature Management Systems because a malfunctioning mixing valve can cause loss of cooling or heating capability during surgery.

    Product
    Terumo HX2 Temperature Management System provides temperature control of two independent water circuits that directly controls the temperature of patient blood and cardioplegia solution during cardiovascular surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1203-2015·2015-02-25

    Condies Foods Recalls Salsa Due to Undeclared Peanut Protein

    Condies Foods is recalling Bold & Zesty Salsa because it contains cumin that may have undeclared peanut protein. The product was distributed in Utah and Idaho.

    Product
    Condies Foods, Bold & Zesty Salsa, 14 oz, UPC: 05077744220
    Category
    Food
    Distribution
    2 states
  • HighCPSC·15721·2015-02-24

    Safe Step Walk-In Tubs Recalled Due to Heated Seat Burn Hazard

    Oliver Fiberglass and NuWhirl Systems are recalling about 6,400 Safe Step walk-in tubs because the heated seat can get stuck on and overheat, posing a burn risk.

    Product
    Safe Step Walk-In Tubs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V107000·2015-02-24

    Prevost Recalls 2014 X3-45 Coaches Due to Seat Belt Defect

    Prevost is recalling 38 model year 2014 X3-45 commuter coaches because the driver's seat belt retractor may not lock properly, increasing injury risk in a crash.

    Product
    PREVOST — PREVOST X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15083·2015-02-24

    Fanimation Recalls Brewmaster Ceiling Fans Due to Falling Hub Risk

    Fanimation is recalling Brewmaster ceiling fans because the hub holding the blades can separate from the shaft, posing a risk of injury to bystanders.

    Product
    Brewmaster Ceiling Fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V100000·2015-02-23

    Hyundai Recalls Elantra Vehicles Due to Power Steering Loss Risk

    Hyundai is recalling 2008-2010 Elantra and 2009-2010 Elantra Touring vehicles because the electronic power steering system may disable, increasing crash risk.

    Product
    HYUNDAI — HYUNDAI ELANTRA TOURING, ELANTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V104000·2015-02-23

    Gulf Stream Recalls 2010-2014 Trailers Due to Incorrect Tire Labels

    Gulf Stream is recalling 2010-2014 Conquest SE, Kingsport, and Trail Master trailers because incorrect tire labels may lead to over-inflation and tire blowouts.

    Product
    GULF STREAM — GULF STREAM CONQUEST SE, KINGSPORT, TRAIL MASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V102000·2015-02-23

    Keystone Recalls 2013-2015 RVs Due to Failing Entry Step Rivets

    Keystone RV Company is recalling 5,390 Montana, Raptor, and Dutchmen Voltage vehicles because entry step rivets may shear, causing the steps to fail and increasing the risk of falls.

    Product
    KEYSTONE — KEYSTONE, DUTCHMEN RAPTOR, MONTANA, VOLTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V101000·2015-02-23

    Altec Recalls 2012-2014 Digger Derrick and Aerial Devices for Fire Risk

    Altec is recalling 2012-2014 Digger Derrick and Aerial Device vehicles mounted on Freightliner chassis because a slow-reacting circuit breaker may cause overheating and fire.

    Product
    ALTEC — ALTEC AERIAL DEVICE, DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V103000·2015-02-23

    Cruiser RV Recalls 2016 Stryker Toy Trailers Due to Exhaust Fume Risk

    Cruiser RV is recalling 2016 Stryker Toy and Stryker Toy Hauler trailers with optional slide floors because occupants may be exposed to exhaust fumes.

    Product
    CRUISER RV — CRUISER RV STRYKER TOY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E012000·2015-02-19

    Meritor Recalls Front Non-Drive Axles Due to Tie Rod Torque Issue

    Meritor is recalling specific front non-drive axles because tie rod nuts may not be properly torqued, which could lead to a loss of vehicle control.

    Product
    STEERING:LINKAGES:TIE ROD ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V097000·2015-02-19

    Hyundai Recalls 2015 Genesis Vehicles for Tail Light Water Leak

    Hyundai is recalling 2015 Genesis vehicles because water may leak into tail lights, causing incorrect gear displays or delayed gear engagement, which increases crash risk.

    Product
    HYUNDAI — HYUNDAI GENESIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V094000·2015-02-19

    Freightliner M2 Brake Warning Recall Due to Switch Incompatibility

    Daimler Trucks is recalling 2015 Freightliner Business Class M2 vehicles because brake warning lights may not illuminate correctly, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1068-2015·2015-02-18

    Fruitful Juice Bloody Mary Beverage Recalled for Undeclared Anchovy Allergen

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

    Product
    Fruitful Juice Products Bloody Mary Beverage, contains 56% Juice. Ready to Use Packed in 5 gal Bag in Box and 36 FL oz. bottles, 12 to a case. glass bottles, 12 per case packed in 3 gal Bag in Box. UPC - 5 gallon bag in box 7 0073 87405 7; UPC Mt. Rose The Lakes 7…
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-1064-2015·2015-02-18

    Virtual Imaging Recalls Digital Mobile X-ray Systems Due to Motion Defect

    Virtual Imaging, Inc. is recalling 316 digital mobile X-ray systems in the US and 6 in Canada due to a potential for unintended and erratic motion.

    Product
    Digital Mobile X-ray Systems used to take diagnostic radiographic exposures or patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1100-2015·2015-02-18

    Teleflex Medical Recalls Aquapak 340 SW Humidifier Adaptors for Foreign Material

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

    Product
    AQUAPAK 340 SW, 340 ML W/040 ADAPTOR, FREN. 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 (Food)·F-1040-2015·2015-02-18

    Son In Law Products Recalls BBQ Sauces for Undeclared Anchovies

    Son In Law Products is recalling Hot & Medium Smoking BBQ, Garlic & Honey horseradish BBQ, and Cherry BBQ Sauces because they contain anchovies not declared on the labeling.

    Product
    Hot Smoking BBQ Sauce
    Category
    Food
    Distribution
    5 states