The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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5251–5275 of 7463

  • SevereFDA (Food)·F-0087-2024·2023-03-22

    Orchard Bistro Egg Salad Kaiser Recalled for Potential Listeria Contamination

    Fresh Ideation Food Group is recalling Orchard Bistro Egg Salad Kaiser (5.5 oz) sold January 24-30, 2023, due to potential Listeria monocytogenes contamination. The product was distributed to multiple states in the Northeast and Mid-Atlantic.

    Product
    Orchard Bistro, Egg Salad Kaiser, Net . Wt. 5.5 Oz. Single Serving, Keep refrigerated
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Food)·F-0135-2024·2023-03-22

    Ham and Cheese Sandwiches Recalled for Potential Listeria Contamination

    Orchard Bistro Ham & Cheese Finger Sandwiches sold in January 2023 are recalled due to potential Listeria monocytogenes contamination. Affected products were distributed to 11 states.

    Product
    Orchard Bistro, Ham & Cheese Finger Sandwiches, Single Serving, Keep refrigerated
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Food)·F-0050-2024·2023-03-22

    Fresh Creative Cuisine Pretzel Baguette Recalled Due to Listeria Risk

    Fresh Creative Cuisine recalled a Black Forest Ham & Muenster Pretzel Baguette distributed across multiple states due to potential Listeria monocytogenes contamination.

    Product
    Fresh Creative Cuisine Tan Label, Black Forest Ham & Muenster Pretzel Baguette, Net Wt. 9 Oz. Single Serving, Keep refrigerated
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Food)·F-0104-2024·2023-03-22

    Quick & Fresh Pineapple Chunks Recalled Due to Listeria Risk

    Fresh cut pineapple chunks from Fresh Ideation Food Group are being recalled for potential Listeria monocytogenes contamination. The affected products were sold January 24–30, 2023 across 11 states.

    Product
    Quick & Fresh, Fresh Cut Pineapple Chunks, Net . Wt. 7 Oz. Single Serving, Keep refrigerated
    Category
    Food
    Distribution
    11 states
  • SevereNHTSA·23V172000·2023-03-16

    2023 Cadillac XT6 Transmission Defect Recall for Half-Shaft Disengagement

    General Motors is recalling 2023 Cadillac XT6 and related vehicles due to a transmission defect. An incorrectly built sun gear can cause the half-shaft to disengage, risking loss of drive power or vehicle rollaway.

    Product
    CADILLAC — 2023 CADILLAC XT6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23734·2023-03-16

    Polaris Sportsman ATVs Recalled for Fire and Brake Loss Hazards

    Polaris is recalling model years 2021–2023 Sportsman 450 and 570 ATVs because an improperly assembled wiring harness can contact the brake line and vehicle frame, resulting in front brake loss and fire.

    Product
    Model Years 2021-2023 Sportsman 450 and 570 All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1148-2023·2023-03-15

    Cardiosave Rescue intra-aortic balloon pump may shut down unexpectedly

    The Cardiosave Rescue intra-aortic balloon pump may suddenly stop working due to communication failure between internal circuit boards, interrupting patient therapy and threatening hemodynamic stability.

    Product
    Cardiosave Rescue Model Nos. 0998-00-0800-75 0998-00-0800-83 0998-00-0800-85
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0455-2023·2023-03-15

    Hand Sanitizer Recalled for Methanol and Acetaldehyde Contamination

    Snowy Range Blue hand sanitizer is recalled due to FDA findings of methanol, acetaldehyde, and acetal above permissible limits. The product was distributed nationwide across all lot codes.

    Product
    Snowy Range Blue Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-Sterile Solution, 4fl. oz. [118mL], Distributed by Reliable Products, LLC, Cheyenne, WY 82003, NDC 75288-100-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1145-2023·2023-03-15

    Cardiosave Hybrid IABP Devices Recalled for Unexpected Shutdown Risk

    Datascope Corp. is recalling Cardiosave Hybrid IABP devices due to a connection failure that may cause unexpected shutdown during use. The failure prevents communication between the device's display head and base unit.

    Product
    Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Containing Coiled Cord cable (part number 0012-00-1801, Model Numbers 0998-00-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-00-0800-53, 0998-00-0800-55, 0998
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0410-2023·2023-03-15

    JSJ Chocolate Cake Recalled for Undeclared Egg Allergen

    Titans Global Inc. is recalling JSJ Chocolate Cake due to undeclared egg not listed on the label. The recall affects 12,432 units distributed to five retail locations in California.

    Product
    JSJ Chocolate Cake 3.35 oz (95g) 28 units per case produced date: 2022/11/08
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0417-2023·2023-03-15

    Chukar Cherries Cherry Bombs Recalled Nationwide for Undeclared Hazelnuts

    Chukar Cherry Company is recalling Cherry Bombs Bits 'n Pieces chocolate candy nationwide due to undeclared hazelnuts, a food allergen.

    Product
    Chukar Cherries Cherry Bombs Bits 'n Pieces, item #21508, net wt. 12 oz. (340g). UPC 0 11261 21508 9. Product is packaged in clear plastic film pouch. INGREDIENTS: Milk, Bittersweet, Semisweet, and White Chocolate (Sugar, Unsweetened Chocolate processed with potassium carbonate
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0412-2023·2023-03-15

    JSJ DMC Leaf Cake recalled due to undeclared egg allergen

    JSJ DMC Leaf Cake (3.35 oz, produced 2022/11/08) has been recalled because egg is present but not declared on the label. The recall affects 12,432 units distributed to 5 retail locations in California.

    Product
    JSJ DMC Leaf Cake 3.35 oz (95g) 28 units per case produced date: 2022/11/08
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0411-2023·2023-03-15

    JSJ ZSR Cake recalled for undeclared egg allergen

    Titans Global Inc. is recalling JSJ ZSR Cake due to undeclared egg on the label. The recall affects 12,432 units distributed to five retail locations in California.

    Product
    JSJ ZSR Cake 3.35 oz (95g) 28 units per case produced date: 2022/11/08
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1147-2023·2023-03-15

    Cardiosave Hybrid IABP Recalled for Risk of Unexpected Shutdown

    The Cardiosave Hybrid intra-aortic balloon pump (IABP) is being recalled because it may unexpectedly shut down due to communication loss between internal components. The shutdown could interrupt therapy in cardiac patients and compromise their hemodynamic stability.

    Product
    Cardiosave Hybrid Model Nos. 0998-00-0800-31 0998-00-0800-32 0998-00-0800-33 0998-00-0800-34 0998-00-0800-35 0998-00-0800-45 0998-00-0800-52 0998-00-0800-53 0998-00-0800-55 0998-00-0800-65 0998-UC-0800-31* 0998-UC-0800-33* 0998-UC-0800-52* 0998-UC-0800-53* 0998
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1146-2023·2023-03-15

    Cardiosave Rescue Intra-Aortic Balloon Pumps recalled for connection failure

    Datascope Corp. is recalling Cardiosave Rescue Intra-Aortic Balloon Pumps due to a coiled cord cable connection failure that may cause unexpected device shutdown and loss of communication.

    Product
    Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Containing Coiled Cord cable (part number 0012-00-1801, Model Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0456-2023·2023-03-15

    Drug Recall: Pharmedica Non-Sterile MSM Drops Due to Contamination

    Pharmedica USA recalled Purely Soothing 15% MSM Drops nationwide due to non-sterility concerns. The voluntary Class I recall affects approximately 1,904 bottles distributed via e-commerce and trade shows.

    Product
    Purely Soothing 15% MSM Drops, packaged in a)15 ml, .5 fl oz bottle, UPC 7 31034 91382 9; and b) 30 ml, 1.014 fl oz bottle, UPC 7 31034 91379 9; Manufactured by: Pharmedica USA, Phoenix, AZ.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V167000·2023-03-15

    2023 Alliance RV Valor travel trailers recalled for incorrect wheel assemblies

    Alliance RV is recalling certain 2023 Valor 21T15 travel trailers with incorrect wheel and tire assemblies that may become overloaded. Overloaded tires can fail and increase the risk of crashes.

    Product
    ALLIANCE RV — 2023 ALLIANCE RV VALOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·23150·2023-03-09

    Calico Critters Animal Figures Recalled Due to Choking Hazard; Two Deaths Reported

    Epoch Everlasting Play is recalling more than 3.2 million Calico Critters animal figures and sets sold with bottle and pacifier accessories due to choking hazard. Two fatal incidents have been reported.

    Product
    Calico Critters® Animal Figures and Sets sold with Bottle and Pacifier Accessories
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23735·2023-03-09

    Bedsure Electric Heating Blankets and Pads Recalled for Fire and Burn Hazards

    Bedsure electric heating blankets and pads are recalled because their controllers can malfunction, causing fires and thermal burns. Consumers should stop using them immediately and contact Bedsure for a refund.

    Product
    Bedsure Electric Heating Blankets and Pads
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1140-2023·2023-03-08

    Life2000 Hospital Ventilator Recalled for Potential Patient Desaturation Risk

    Baxter Healthcare is recalling 135 Life2000 ventilators nationwide due to potential patient desaturation when connected to an oxygen concentrator.

    Product
    Life2000 Ventilator PKG, Hospital, a) REF BT20007, b) REF BT-20-0007, ventilatory support for the care of individuals
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V155000·2023-03-08

    Ford Recalls 2022-2023 Bronco for Steering Gear Lock-Up Defect

    Ford recalls 2022-2023 Broncos for steering gear damage that can lock up the steering wheel and cause loss of steering control, increasing crash risk.

    Product
    FORD — 2022 FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1141-2023·2023-03-08

    Life2000 Hospital Ventilator Recalled for Patient Desaturation Risk

    Baxter Healthcare is recalling 8 Life2000 Hospital Ventilator systems due to potential patient desaturation events when the device is connected to an oxygen concentrator.

    Product
    Life2000 Ventilator PKG, Hospital, a) REF BT200011, b) REF BT-20-0011, ventilatory support for the care of individuals
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V154000·2023-03-08

    2023-2024 International trucks recalled for loose battery box bolts

    Navistar is recalling certain 2023 and 2024 International trucks because battery box mounting bolts may be loose or missing. Loose bolts could allow the battery box to detach, creating a road hazard and increasing crash risk.

    Product
    INTERNATIONAL — 2023 INTERNATIONAL MV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0453-2023·2023-03-08

    PrimeZEN Black 6000 Capsule Recalled for Undeclared Pharmaceutical Ingredients

    The FDA is recalling PrimeZEN Black 6000 capsules distributed nationwide because they contain undeclared sildenafil and tadalafil. The product is unapproved and was marketed without FDA authorization.

    Product
    PrimeZEN Black 6000 capsule, 2000mg, Male Sexual Performance Enhancement, 1-count blister card, Distributed by: Prime Premier Group, Los Angeles, CA 90006, UPC 7 28175 52189 1.
    Category
    Drug
    Distribution
    Distributed nationwide