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 the agency’s own highest classification or reported deaths or serious injuries, 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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11051–11075 of 89674

  • HighFDA (Food)·F-1775-2024·2024-09-11

    Reser's Homestyle Gravy Recalled Due to Temperature Abuse

    Reser's Fine Foods recalls Item 71117.14459 Gravy Homestyle due to temperature abuse during shipping. The product may become spoiled and pose food safety risks.

    Product
    Item 71117.14459, Gravy Homestyle, refrigerated product, net wt. 4lb. There are 3 packs per case.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-2948-2024·2024-09-11

    BD Pyxis QFill Medication Cabinet Software Bug Causes Incorrect Restock Labels

    The BD Pyxis QFill Replenishment Station medication cabinet has a software issue that may print incorrect bin information on restock labels for medications stored in non-CUBIE locations.

    Product
    BKIT BD Pyxis QFill Replenishment Station, REF: 155197-01, medication cabinet system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2955-2024·2024-09-11

    Impella CP Smart Assist Set Lacks Labeling for Potential Device Interaction

    Abiomed is updating labeling for the Impella CP Smart Assist Set to warn about a potential interaction with the Shockwave Coronary IVL Catheter when used during coronary interventions. The interaction was previously undocumented in the device instructions.

    Product
    Impella CP Smart Assist Set, JP; Product Code: 0048-0024-JP;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2956-2024·2024-09-11

    Impella CP Pump Set Recalled for Potential Device Interaction

    Abiomed is recalling the Impella CP Pump Set due to a potential device interaction with the Shockwave Coronary IVL Catheter during coronary interventions. The manufacturer will update device instructions to address this interaction.

    Product
    Impella CP Pump Set, Japan; Product Code: 0048-0034-JP;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2964-2024·2024-09-11

    Pump 381 Pump Set lacks labeling for Shockwave catheter interaction risk

    Abiomed's Pump 381 Pump Set labeling lacks information about potential interactions with Shockwave Coronary IVL Catheters during coronary interventions. The manufacturer is updating instructions for use to address this gap.

    Product
    Pump 381 Pump Set (US); Product Code: 1000080;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1782-2024·2024-09-11

    Pita Jungle Greek Salad Recalled for Undeclared Milk Allergen

    SSP America PHX, LLC recalls Pita Jungle Greek Salad (11.8oz clamshell) because the product label listed feta but failed to declare milk as an allergen. Consumers with milk allergies should not consume this product.

    Product
    Pita Jungle Greek Salad packaged in 11.8oz plastic clamshell container.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1786-2024·2024-09-11

    Cheese Danish Recalled for Undeclared Milk Allergen

    SSP America PHX, LLC is recalling Cheese Danish pastries distributed in Arizona. The product labels list cheese but fail to declare milk in the allergen statement, posing a risk to consumers with milk allergies.

    Product
    Cheese Danish in a clear plastic bag with a white paper label attached to the top of the plastic bag.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1795-2024·2024-09-11

    Apple Juice Brands Recalled for Inorganic Arsenic Contamination Above FDA Action Level

    Multiple apple juice brands sold nationwide are being recalled due to inorganic arsenic levels above FDA action thresholds. The recall affects approximately 141,298 cases sold by Refresco Beverages US Inc.

    Product
    a.) Great Value 8oz Apple Juice in 6pack; PET plastic bottle b.) Great Value 96oz Apple Juice; PET plastic bottle c.) Market Basket 100% apple juice; 64 oz; PET plastic bottle d.) Nice! 100% apple juice ; 64 oz; PET plastic bottle e.) Weis 100% apple juice; 64 oz; PET…
    Category
    Food
    Distribution
    16 states
  • HighFDA (Food)·F-1776-2024·2024-09-11

    Reser's Raspberry Parfait Desserts Recalled for Potential Spoilage

    Reser's Fine Foods recalls 18 cases of Raspberry Parfait Desserts due to temperature abuse during transport that may have caused spoilage. Products with use-by date 12/4/2024 distributed in CA, IL, MN, ND, and SD.

    Product
    Item 71117.15207, Reser's Raspberry Parfait Desserts, refrigerated product, net wt. 8lb. There are 2 packs per case.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1787-2024·2024-09-11

    Apple Danish Recalled for Incorrect Almond Croissant Ingredient Labeling

    SSP America PHX is recalling Apple Danish products due to incorrect ingredient labeling. The label lists Almond Croissant ingredients instead of Apple Danish, creating a risk for consumers with tree nut allergies.

    Product
    Apple Danish in a clear plastic bag with a white paper label attached to the top of the plastic bag.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0650-2024·2024-09-11

    Compounded semaglutide injection recalled due to sterility concerns

    ProRx LLC is recalling compounded semaglutide injections due to lack of assurance of sterility. The recall affects 2,490 vials distributed nationwide.

    Product
    Semaglutide, 2 mL (2.5mg/mL), Compounded RX Product, Multidose SC inj, glass vial, ProRx, 267-565-7008, NDC 84139-225-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2965-2024·2024-09-11

    Impella 5.5 Device Recalled for Missing Labeling on Catheter Interaction

    Abiomed is updating labeling for Impella 5.5 cardiac support pumps to include information about a potential device interaction with Shockwave Coronary IVL Catheters during coronary interventions.

    Product
    Impella 5.5 with SmartAssist S2 Set, US; Product Code: 1000100;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1771-2024·2024-09-11

    Reser's Smokehouse Potato Salad Recalled Due to Spoilage Risk

    Reser's Fine Foods is recalling 7 cases of Smokehouse Potato Salad due to potential spoilage from temperature abuse during shipping. No illnesses have been reported.

    Product
    Item 71117.10923, Reser's Smokehouse Potato Salad, refrigerated product, net wt. 5lbs. There are 2 packs per case.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-2980-2024·2024-09-11

    Beckman Power Express Centrifuge Sample Holder May Detach During Operation

    An adhesive joint failure in the PE Centrifuge Temperature Controlled component can cause the metal part to detach inside the centrifuge, risking sample destruction and potential exposure of laboratory technicians to biohazardous material.

    Product
    PE Centrifuge Temperature Controlled, REF: B36366, a component of the Power Express.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2945-2024·2024-09-11

    Heparin Gore Viabahn VBX Endoprosthesis Recalled for Packaging Defects

    W L Gore & Associates is recalling Heparin Gore Viabahn VBX Balloon Expandable Endoprosthesis devices due to packaging defects that may compromise sterility assurance and heparin activity.

    Product
    Heparin, Gore Viabahn VBX, Balloon Expandable Endoprosthesis, for the following Reference numbers: United States: BXB051501A BXB051502A BXB051901A BXB051902A BXB052901A BXB052902A BXB053901A BXB053902A BXB055901A BXB055902A BXB057901A BXB057902A BXB061501A BXB061502A…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0651-2024·2024-09-11

    Compounded Tirzepatide Injectable Vials Recalled for Sterility Assurance Issues

    ProRx LLC is recalling 37 vials of compounded Tirzepatide injectable due to lack of sterility assurance. The 2 mL vials (10 mg/mL and 20 mg/mL) were distributed nationwide.

    Product
    Tirzepatide 2 mL (10 mg/mL) and 20 mg/mL, 2mL Multidose SC Injection vials, Compounded Rx Product, ProRx 267-565-7008, NDC 84139-210-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2979-2024·2024-09-11

    Power Express PE Centrifuge adhesive joint failure may cause component detachment

    The adhesive joint in this medical device component can fail, causing the metal part to detach. This may damage the centrifuge, destroy patient samples, and potentially expose lab staff to biohazardous material.

    Product
    PE Centrifuge, REF: B36365, a component of the Power Express
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V667000·2024-09-11

    Ember Recalls 2023-2024 Travel Trailers Due to Incorrect Cargo Capacity Labels

    Ember is recalling 2023-2024 E-Series, Overland Series, and Touring Edition travel trailers because certification labels list incorrect cargo carrying capacity, which can allow the trailer to become overloaded.

    Product
    EMBER — EMBER E-SERIES, OVERLAND SERIES, TOURING EDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1769-2024·2024-09-11

    Reser's Banana Pudding Kit Recalled Due to Temperature Abuse

    Reser's Fine Foods recalls 6 cases of Item 71117.03034 Banana Pudding Kit due to temperature abuse from a malfunctioning refrigeration unit. Affected products were distributed to CA, IL, MN, ND, and SD.

    Product
    Item 71117.03034, Reser's Kit HF Pudding Banana, refrigerated product, net wt. 4.81lb. There are 2 packs per case.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-2946-2024·2024-09-11

    W L Gore Recalls Heparin Viabahn VBX Endoprosthesis Due to Packaging Defects

    W L Gore & Associates is recalling specific lots of Heparin, Gore Viabahn VBX Balloon Expandable Endoprosthesis because packaging defects may compromise sterility and heparin activity.

    Product
    Heparin, Gore Viabahn VBX, Balloon Expandable Endoprosthesis, for the following Reference numbers: United States: BXB055902C, BXB063902C, BXB065902C, BXB067902C, BXB073902C, BXB075902C, BXB077902C, BXB083902C, BXB085902C, BXB087902C, BXB093902C, BXB095902C, BXB097902C…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V666000·2024-09-10

    Thor Motor Coach Recalls 2024 Motorhomes Due to Overheating Propane Tank Risk

    Thor Motor Coach is recalling 2024 Palladium and Talavera motorhomes because the liquid propane tank is located too close to the chassis exhaust, creating a fire risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TALAVERA, PALLADIUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V668000·2024-09-10

    Freightliner and Western Star brake lights may fail during emergency braking

    Daimler Trucks is recalling certain Freightliner and Western Star trucks because brake lights may fail to illuminate during automatic emergency braking, increasing crash risk. Dealers will update software at no cost.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR EM2, 57X, 47X, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide