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.

26801–26825 of 50462

  • HighNHTSA·18V878000·2018-12-10

    Thomas Built Buses Saf-T-Liner C2 Recalled for Roof Adhesive Defect

    Daimler Trucks North America is recalling 2017-2019 Thomas Built Buses Saf-T-Liner C2 transit buses because improperly applied roof adhesive may increase injury risk in rollover crashes.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V874000·2018-12-07

    Rosenbauer Fire Apparatus Recalled for Brake Light Wiring Defect

    Rosenbauer America is recalling 2017-2018 Fire Apparatus vehicles because Whelen accessory brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.

    Product
    ROSENBAUER — ROSENBAUER FIRE APPARATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V873000·2018-12-07

    Altec Recalls 2017-2018 Vehicles Due to Brake Light Wiring Defect

    Altec is recalling 2017-2018 Aerial Devices, Service Bodies, and Digger Derricks because Whelen accessory brake lights may illuminate without the brake pedal being pressed.

    Product
    ALTEC — ALTEC AERIAL DEVICE, SERVICE BODY, DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V871000·2018-12-07

    Keystone Recalls 2018-2019 Raptor Trailers Due to Propane Line Routing

    Keystone RV Company is recalling 2018-2019 Raptor recreational trailers because an incorrectly routed propane line allows the grill to be stored while lit, increasing fire risk.

    Product
    KEYSTONE — KEYSTONE RAPTOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19044·2018-12-06

    Meijer Recalls Falls Creek Kids Hoodies Due to Choking Hazard

    Meijer is recalling about 25,000 Falls Creek Kids infant and toddler hoodies because the zipper slider can detach, posing a choking hazard to young children.

    Product
    Falls Creek Kids infant and toddler hoodies
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19042·2018-12-06

    Skip Hop Recalls Tuo Convertible High Chairs Due to Fall Hazards

    Skip Hop is recalling Tuo convertible high chairs because the legs can detach from the seat, posing fall and injury hazards to children.

    Product
    Tuo convertible high chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V868000·2018-12-06

    GM Recalls 2019 Silverado and Sierra Crew Cab for Air Bag Defect

    General Motors is recalling 2019 Chevrolet Silverado 1500 and GMC Sierra 1500 Crew Cab vehicles because the passenger-side air bag may not inflate properly in a crash.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 1500, SIERRA 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0521-2019·2018-12-05

    GE Healthcare Recalls Dash 5000 Patient Monitoring Systems

    GE Healthcare is recalling approximately 182,640 Dash 5000 Patient Monitoring Systems because they may simultaneously restart during prolonged network overloads.

    Product
    Dash 5000 Patient Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0670-2019·2018-12-05

    Shirleys Chocolate Whoopie Pies Recalled for Undeclared Peanut Allergen

    Shirleys Cookie Company is recalling Chocolate Peanut Butter Whoopie Pies labeled as Chocolate Whoopie Pies because the peanut allergen is not declared on the packaging.

    Product
    Weis Chocolate Whoopie Pie 16 oz (454g)/ 4 4 oz Whoopie Pies Clamshell Packaging 4 Whoopie Pies per Unit
    Category
    Food
    Distribution
    0 states
  • HighFDA (Drugs)·D-0287-2019·2018-12-05

    Ascend Recalls Quetiapine Tablets Due to Metal Shard Contamination

    Ascend Laboratories is recalling Quetiapine 400 mg tablets because a metal shard was found in a tablet. Patients should stop using the affected lot and contact their healthcare provider.

    Product
    QUETIAPINE — QUETIAPINE (QUETIAPINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0719-2019·2018-12-05

    Pictsweet Farms Steam'ables Asparagus Spears Recalled for Listeria

    Hart Freeze pack, LLC is recalling Pictsweet Farms Steam'ables Asparagus Spears because the product tested presumptive positive for Listeria monocytogenes.

    Product
    Pictsweet Farms Steam'ables Asparagus Spears 8oz. pouch, 10 per case UPC 0 70560 97799 9 Frozen
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0524-2019·2018-12-05

    GE Healthcare Recalls Solar 9500 Patient Monitors Due to Network Overload Risk

    GE Healthcare is recalling approximately 3,864 Solar 9500 Information Monitoring Systems because they may simultaneously restart if connected to the same network during a prolonged network overload.

    Product
    Solar 9500 Information Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0523-2019·2018-12-05

    GE Healthcare Recalls Solar 8000M Patient Monitoring Systems

    GE Healthcare is recalling Solar 8000M patient monitors because they may restart simultaneously during network overload, potentially disrupting patient monitoring.

    Product
    Solar 8000M Patient Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0522-2019·2018-12-05

    GE Healthcare Recalls Solar 8000i Patient Monitoring Systems

    GE Healthcare is recalling approximately 73,673 Solar 8000i and 8000M patient monitoring systems because they may simultaneously restart during prolonged network overloads.

    Product
    Solar 8000i Patient Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0518-2019·2018-12-05

    Fresenius Granuflo Dry Acid Concentrate Recalled for Foreign Substance

    Fresenius Medical Care is recalling Granuflo Dry Acid Concentrate for hemodialysis due to confirmed foreign substance contamination.

    Product
    Fresenius Granuflo Dry Acid Concentrate- 3K 2.5 Ca 1 Mg 16.5 GAL Catalog Number: OFD3251-3B for hemodialysis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0501-2019·2018-12-05

    NxStage PureFlow B Solution Recalled Due to Bag Burst Risk

    NxStage Medical is recalling PureFlow B Solution because the smaller chamber of the two-chamber bag can burst, releasing electrolyte fluid that may injure eyes or skin.

    Product
    NxStage PureFlow B Solution-RFP-401, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0677-2019·2018-12-05

    Duncan Hines Confetti Cake Mix Recalled for Salmonella

    ConAgra Foods is recalling Duncan Hines Signature Confetti Cake Mix after a positive finding of Salmonella in a retail sample.

    Product
    Duncan Hines Signature Confetti Cake cake mix 15.25oz. 12 retail units per case 644209414550
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0672-2019·2018-12-05

    Finax Muesli Recalled for Missing Coconut Allergen Labeling

    Chicago Importing Co is recalling Finax Muesli with 45% Fruit because the ingredients statement does not indicate the presence of coconut.

    Product
    Finax Muesli with 45% Fruit; 22.9-oz.; Heat sealed plastic bag; 10 bags/case
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-0676-2019·2018-12-05

    Duncan Hines Cake Mix Recalled for Salmonella Contamination

    ConAgra Foods is recalling Duncan Hines Classic Butter Golden cake mix due to a positive Salmonella finding in a retail sample.

    Product
    Duncan Hines Classic Butter Golden cake mix 15.25oz. 12 retail units per case 644209307593
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0285-2019·2018-12-05

    Germ Bloc Health Hand Sanitizer Foam Recalled for Pseudomonas Contamination

    AVKARE Inc. is recalling specific lots of Germ Bloc Health Hand Sanitizer Foam due to the presence of Pseudomonas aeruginosa.

    Product
    Germ Bloc Health Hand Sanitizer Foam (benzalkonium chloride 0.13%) 7.5fl.oz./222mL refill bags, AvKARE, Inc. Pulaski, TN 38478 www.avkare.com, NDC 5026835427, UPC 3 50268 35408
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Food)·F-0669-2019·2018-12-05

    Kroger Southwest Sweet Potato Rice Recalled for Potential Pathogen Contamination

    Mary's Harvest Fresh Foods is recalling Kroger Southwest Sweet Potato Rice due to potential contamination with Salmonella or Listeria monocytogenes.

    Product
    Refrigerated Kroger Southwest Sweet Potato Rice 12 oz. UPC # 826766185610. In rigid plastic container. Label has cooking instructions which states: Heat vegetable oil until very hot in large saute pan. Toss in vegetable and stir fry 1 minute.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0515-2019·2018-12-05

    Eurotrol HemoTrol Level 3 Recalled Due to Microbial Contamination

    Eurotrol Inc. is recalling HemoTrol Level 3 hematology quality control mixtures because microbial contamination causes incorrect, lower-than-assigned measurement results.

    Product
    HemoTrol Level 3- In Vitro Diagnostic Hematology quality control mixture. Catalogue number: 171.003.002 Eurotrol HemoLin is an assayed hemoglobin control intended for professional use in the verification of the linearity of the HemoCue¿ Hb 201 systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide