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.

16976–17000 of 53124

  • HighFDA (Food)·F-1305-2022·2022-06-22

    White Cane Sockeye Salmon Recall: Undeclared Wheat and Soy Allergens

    White Cane Sockeye Salmon packages contain undeclared wheat and soy in the teriyaki sauce. Consumers with allergies to these allergens should not consume this product.

    Product
    Wild Alaskan Cooked and Smoked Salmon, brand White Cane Sockeye Salmon, 4-6 oz. is packaged in a vacuum sealed bag. The label is read in parts: "***WILD ALASKAN COOKED AND SMOKED SALMON *** Ingredients: Salmon, Teriyaki Sauce, Brown Sugar, Olive Oil, Sea Salt and Garlic…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1260-2022·2022-06-22

    Illumina NextSeq 550 Genetic Sequencer Cybersecurity Vulnerability Recall

    Illumina is recalling 799 NextSeq 550 Dx genetic sequencers due to a cybersecurity vulnerability in the Local Run Manager software. Affected devices have been distributed worldwide and in the United States.

    Product
    illumina Model NextSeq 550 Dx REF 20005715
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1263-2022·2022-06-22

    Olympus Uretero-Reno Fiberscope Recalled for Defective Adhesive and Vision Loss

    The Olympus URETERO-RENO FIBERSCOPE Model URF-P6 is recalled for incorrect adhesive securing the diopter ring. The defect may cause loss of adjustment function, blurred vision, and in rare cases, urinary tract perforation.

    Product
    Olympus URETERO-RENO FIBERSCOPE Model: URF-P6
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Food)·F-1377-2022·2022-06-22

    Finest Traditions Smokey Baked Beans recalled for potential metal contamination

    Morski Brands, Inc. is recalling 2,648 units of Finest Traditions Smokey Baked Beans due to the potential presence of foreign metal objects. The recalled product was distributed nationwide.

    Product
    Finest Traditions Smokey Baked Beans, #1038700, Net Wt 8 lb (3.63 kg) Keep Refrigerated UPC 10 7 33147 10231 9. Distributed By: DBC Foods, St Cloud, MN 56302
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·22V442000·2022-06-22

    2022 Grand Design Momentum Travel Trailer Electrical Fire Hazard Recall

    Grand Design is recalling 165 model-year 2022 Momentum travel trailers due to improper 110-volt electrical wiring that can overheat and create a fire risk. Dealers will rewire the power supply at no cost.

    Product
    GRAND DESIGN — GRAND DESIGN MOMENTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1378-2022·2022-06-22

    Potato Salad Recalled Nationwide for Metal Contamination Risk

    Morski Brands recalled 832 units of Dawn's Smoked Gouda & Bacon Potato Salad due to possible metal fragments. Consumers with products bearing best-before dates 5-13-22, 6-21-22, 6-24-22, or 6-27-22 should not consume them.

    Product
    Dawn's Smoked Gouda & Bacon Potato Salad, #10079, Net Wt 8 lb (3.63 kg) Keep Refrigerated. UPC 10032345130019. Mfg By Morski Brands, Inc., Portage, WI 53901
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1144-2022·2022-06-22

    Medroxyprogesterone Acetate Injectable Suspension Recalled for Sterility Assurance Failure

    Sun Pharmaceutical is recalling medroxyprogesterone acetate injectable suspension due to lack of assurance of sterility. The recall affects approximately 57,997 prefilled syringes distributed nationwide.

    Product
    medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150 mg/mL, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Sun Pharmaceutical Industries Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 16714-999-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V440000·2022-06-21

    Fabform Recalls 2018-2022 Trailers Due to Utility Gate Stop Defect

    Fabform is recalling 2018-2022 FLR-D, FLRR-D, and DBX trailers because a rubber stop may break, allowing the utility gate to detach and increase crash risk.

    Product
    FABFORM — FABFORM FLRR-D, DBX, FLR-D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V438000·2022-06-20

    School Bus Engine Control Module Defect May Cause Unexpected Shutdown

    Daimler Trucks recalls certain Thomas Built school buses (2020-2023) due to an engine control module defect that can cause unexpected engine shutdown while driving, increasing crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E051000·2022-06-20

    BorgWarner Recalls EGR Valves Due to Risk of Loss of Drive Power

    BorgWarner is recalling specific EGR valves where a loose washer may cause the valve to stick open, resulting in an unexpected loss of drive power.

    Product
    ENGINE AND ENGINE COOLING:EXHAUST SYSTEM:EMISSION CONTROL:GAS RECIRCULATION VALVE (EGR VALVE) recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V433000·2022-06-17

    2022 Cruiser RV Travel Trailers Recalled for Cracked LP Gas Fittings

    Cruiser RV is recalling 2022 travel trailers with potentially cracked LP gas system fittings that may leak, creating a fire hazard. Dealers will inspect and replace affected fittings free of charge.

    Product
    CRUISER — CRUISER, CRUISER RV STRYKER, EMBRACE, MPG, RADIANCE ULTRA-LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V437000·2022-06-17

    2019-2022 Autocar Xpeditor Trucks: Water Intrusion in Fuse Box

    Autocar is recalling 2019-2022 Xpeditor trucks due to water intrusion in the external fuse box, which may short circuit and cause unexpected vehicle stalls, increasing crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V434000·2022-06-17

    2022 Isuzu N-Series trucks recalled for incorrectly wired oil pressure sensor

    Isuzu is recalling certain 2022 N-Series trucks with 6.0L engines for incorrectly wired oil pressure sensor assemblies. The defect prevents driver alerts to low oil pressure, risking engine stall and crashes.

    Product
    ISUZU — ISUZU N-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22161·2022-06-16

    Walgreens Acetaminophen Bottles Recalled for Non-Compliant Packaging

    Aurohealth recalled Walgreens brand acetaminophen 500 mg bottles (150 count) because the packaging does not meet child-resistant requirements under the Poison Prevention Packaging Act, posing a poisoning risk to young children.

    Product
    Walgreens Pain Reliever Acetaminophen, 150 count bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·22164·2022-06-16

    Kroger Arthritis Pain Acetaminophen Recalled for Non-Child-Resistant Packaging

    Kroger-brand acetaminophen tablets in 225-count bottles lack required child-resistant packaging, posing a poisoning risk to young children if ingested. About 25,660 units were sold nationwide from December 2021 through March 2022.

    Product
    Kroger Arthritis Pain Acetaminophen, 225 count bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·22162·2022-06-16

    Kroger Acetaminophen Recalled for Non-Child-Resistant Packaging

    Sun Pharmaceutical is recalling Kroger brand acetaminophen 650 mg extended-release caplets because the packaging does not meet child-resistant requirements under the Poison Prevention Packaging Act, posing a risk of poisoning if swallowed by young children.

    Product
    Kroger Acetaminophen, 100 count bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·22166·2022-06-16

    Times Tienda Children's Desks and Chairs Lead Paint Violation

    Times Tienda is recalling approximately 700 children's desks and chairs sold in Puerto Rico because the surface paint contains lead levels that exceed federal bans. Lead poisoning poses a serious health risk to young children.

    Product
    Children's Desks and Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22165·2022-06-16

    Children's Pajamas Recalled for Flammability Hazard and Burn Risk

    Loulou Lollipop children's pajamas fail to meet federal flammability standards for tight-fitting sleepwear, posing a risk of burn injuries. About 1,300 units were sold nationwide online and at children's boutiques from November 2021 through May 2022.

    Product
    Children's pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V428000·2022-06-16

    2022-2023 International Commercial Trucks and Buses Steering Gear Defect

    Navistar is recalling 2022-2023 International commercial vehicles with defective steering gears that may fracture and cause loss of steering control. Contact your dealer or Navistar at 1-800-448-7825 for inspection and free replacement.

    Product
    INTERNATIONAL — INTERNATIONAL, IC BUS HX, LT, RH, LONESTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22160·2022-06-16

    Kroger Aspirin and Ibuprofen Recalled for Lack of Child-Resistant Packaging

    Time-Cap Labs is recalling Kroger-brand aspirin and ibuprofen products because the bottles lack child-resistant packaging required by law, posing a poisoning risk to young children who may swallow the contents.

    Product
    Kroger Aspirin, 300 count bottles and Ibuprofen, 160 count bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·22159·2022-06-16

    Schneider Electric Electrical Panels Recalled for Fire and Burn Hazards

    Schneider Electric is recalling about 1.4 million Square D QO Plug-on-Neutral Load Centers because they can overheat, creating thermal burn and fire hazards. The company is contacting purchasers and installers to arrange free inspections and repairs.

    Product
    Square™ D QO™ Plug-on-Neutral Load Centers, also known as, Load Centers, Breaker Boxes, Electrical Panels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V427000·2022-06-16

    2022 Cadillac XT6 rear suspension toe link separation risk recall

    General Motors is recalling certain 2022 Cadillac XT6, XT5, and GMC Acadia vehicles due to improperly tightened left-rear suspension toe links that may separate, potentially causing loss of vehicle control and crash risk.

    Product
    GMC — GMC, CADILLAC ACADIA, XT6, XT5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1186-2022·2022-06-15

    Elite Mix Chocolate with Wafer Rolls Recalled for Salmonella Contamination Risk

    Elite Mix Chocolate with Wafer Rolls and Coconut, UPC 815871015455, is being recalled nationwide due to potential Salmonella contamination. Consumers should not consume the product and return it to the place of purchase.

    Product
    ELITE MIX CHOCOLATE WITH WAFER ROLLS AND COCONUT UPC: 815871015455 Net Wt. 3.35 oz (95g). Red packaging.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1088-2022·2022-06-15

    Levofloxacin 500 mg Tablets Recalled Due to Manufacturing Temperature Abuse

    Mckesson Medical-Surgical is recalling Levofloxacin 500 mg tablets nationwide due to temperature abuse during manufacturing that violated pharmaceutical quality standards.

    Product
    LEVOFLOXACIN — LEVOFLOXACIN (LEVOFLOXACIN)
    Category
    Drug
    Distribution
    Distributed nationwide