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.

38801–38825 of 50506

  • HighFDA (Food)·F-2143-2015·2015-05-13

    Trader Joe's A Dozen Sweet Bites Recalled for Undeclared Coconut

    Prolainat is recalling Trader Joe's A Dozen Sweet Bites cakes due to undeclared coconut, a major food allergen.

    Product
    TRADER JOES A Dozen Sweet Bites Chocolate and Coffee Opera Cake, Raspberry Macaroon Cake, Caramel & Chocolate Cake, 9.16 oz UPC 00967679 or SKU 096767.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-2191-2015·2015-05-13

    Sazon Coriander & Annatto Low Sodium Recalled for Undeclared Peanut

    Sazon, Inc. is recalling Sazon Coriander & Annatto Low Sodium because the product contains undeclared peanut protein. Consumers with peanut allergies should not consume the product.

    Product
    Sazon Coriander & Annatto Low Sodium
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1583-2015·2015-05-13

    Siemens Axiom Aristos FX Radiography System Cable Cart Recall

    Siemens is recalling 43 Axiom Aristos FX radiography systems because a cable cart defect could cause the cable holder to drop and hit patients or operators.

    Product
    AXIOM ARISTOS FX; Multipurpose Radiography System (MPRS) is a dedicated x-ray system with a flat panel detector which allows the acquisition of x-ray exposures without the use of conventional film/screen systems. The MPRS allows radiographic exposures of the whole body including…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1582-2015·2015-05-13

    Brainlab ExacTrac 6.x Software Recalled for Potential Positioning Errors

    Brainlab AG is recalling ExacTrac 6.x software due to potential patient positioning errors when using CBCT at non-zero couch angles.

    Product
    ExacTrac 6.x. is software used to place patients at an accurately defined point within the treatment beam of a medical accelerator for stereotactic radiosurgery or radiotherapy procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1565-2015·2015-05-13

    Stryker Recalls Wound Drains for Potential Sterility Breach

    Stryker Instruments is voluntarily recalling CBCII Wound Drains and Ambulating Bulbs due to a potential sterility breach in the packaging.

    Product
    1/8 in. Double Trocar with Wound Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound drain has a curved metal trocar attached to one end of the flexible wound drain tube. There is also a polymeric trocar guard that provides protection…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1594-2015·2015-05-13

    ICU Medical Recalls MicroClave T-Connectors Due to Connection Separation Risk

    ICU Medical is recalling MicroClave T-Connectors because potential connection separation issues could lead to leakage.

    Product
    98" (249 cm) Transfer Set w/MicroClave T-Connector, Check Valve, Anti-Siphon Valve, Trifuse Ext Set w/2 MicroClave, Rotating Luer, Non-DEHP Tubing, Item No. B3338 Product Usage: IV Administration sets are intended for the infusion and withdrawal of fluids. The devices are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2157-2015·2015-05-13

    Spiceco Recalls Sylvia's Sizzlin' Hot Spice for Undeclared Peanut

    Spiceco is recalling Sylvia's Sizzlin' Hot Spice because it may contain undeclared peanut protein. The recall includes additional products using the implicated paprika.

    Product
    Sylvia's Sizzlin' Hot Spice, Net Wt. 5.5 oz. (156g), Distributed by: Sylvia Woods Food Company, P.O. Box 240, Harlem, NY 10027, UPC 608623000515
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2159-2015·2015-05-13

    Spiceco Recalls Fiesta Seasoned Salt for Undeclared Peanut

    Spiceco is recalling Fiesta Seasoned Salt because it may contain undeclared peanut protein. The recall includes additional products using the implicated paprika.

    Product
    Fiesta Seasoned Salt Net Wt 16 oz (1 LB) 454 g Distributed By Fiesta Mart Houston TX 77246-7481
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1591-2015·2015-05-13

    ICU Medical Recalls MicroClave T-Connectors Due to Connection Separation Risk

    ICU Medical is recalling specific MicroClave T-Connectors because they may separate, causing fluid leakage.

    Product
    113" (287cm) Transfer Set w/MicroClave T-Connector, Check Valve, Anti-Siphon Valve, Smallbore Quadfuse Ext Set w/MicroClave, 4 Clamps (Blue, 2 Red, White), Rotating Luer, Non-DEHP Tubing, Item No. B33303 Product Usage: IV Administration sets are intended for the infusion and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1590-2015·2015-05-13

    ICU Medical Recalls MicroClave T-Connectors Due to Connection Separation

    ICU Medical is recalling 1,500 MicroClave T-Connectors because potential connection separation issues could lead to leakage.

    Product
    104" (264 cm) Transfer Set w/MicroClave T-Connector, Check Valve, Smallbore Trifuse Ext w/2 MicroClave, Anti-Siphon Valve, 3 Clamps (White, Red, Blue), Rotating Luer, Non-DHEP Tubing, Item No. B33065 Product Usage: IV Administration sets are intended for the infusion and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2164-2015·2015-05-13

    Spiceco Recalls Sweet Hungarian Paprika for Undeclared Peanut

    Spiceco, Inc. is recalling Pride of Szeged Sweet Hungarian Paprika and other products because they may contain undeclared peanut protein.

    Product
    Maison Royal labeled as ordered
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1592-2015·2015-05-13

    ICU Medical Recalls MicroClave T-Connectors Due to Connection Separation Risk

    ICU Medical is recalling 13,800 MicroClave T-Connectors because potential connection separation issues could lead to leakage.

    Product
    108" (274 cm) Transfer Set w/Check Valve, MicroClave T-Connector, Anti-Siphon Valve, Clamp, Luer Lock, Non-DEHP Tubing, Item No. B33326
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V282000·2015-05-13

    Dodge Challenger Recall for Loose Side Air Bag Mounting Bolt

    Chrysler is recalling 2015 Dodge Challengers because a loose or missing rear mounting bolt on the driver's side air bag curtain may increase injury risk in a crash.

    Product
    DODGE — DODGE CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2168-2015·2015-05-13

    Spiceco Recalls Chicken Seasoning and Paprika for Undeclared Peanut

    Spiceco is recalling Better Valu Chicken Seasoning and Pride of Szeged Sweet Hungarian Paprika because they may contain undeclared peanut protein.

    Product
    Better Valu Chicken Seasoning Net. Wt. 5.25 oz (149 g) Distributed by: Federated Group, Inc. 3025 W. Salt Creek Lane Arlington Heights, IL 6005 www.better-valu.com UPC 079807003794
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·15V277000·2015-05-12

    Blue Bird Recalls 2016 School Buses for Seat Flammability Defect

    Blue Bird is recalling 2016 Vision and All American school buses because seat foam may not meet federal flammability standards, increasing fire risk.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15731·2015-05-12

    La-Z-Boy Recalls PowerReclineXRw Furniture Due to Fall Hazard

    La-Z-Boy is recalling about 2,600 PowerReclineXRw recliners and loveseats because they can tip forward when reclined, posing a fall hazard.

    Product
    PowerReclineXRw
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V276000·2015-05-12

    MCI D4000 and D4500 Motorcoaches Recalled for Engine Fire Risk

    Motor Coach Industries is recalling 2011-2012 D4000 and 2014-2015 D4500 motorcoaches because a vent tube defect may allow engine oil to contact hot surfaces, increasing fire risk.

    Product
    MCI — MCI D4500, D4000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V273000·2015-05-11

    Forest River Recalls Trailers Due to Failing Entry Step Rivets

    Forest River is recalling specific 2013-2015 RV trailers because a rivet on the quad entry steps may shear, causing the steps to fail and increasing the risk of injury.

    Product
    FOREST RIVER — FOREST RIVER CEDAR CREEK, DYNAMAX, SIERRA, CARDINAL
    Category
    Vehicle
    Distribution
    Distributed nationwide