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.

Filters

Agency

Category

Minimum severity

Clear filters

1376–1400 of 5642

  • SevereFDA (Devices)·Z-1274-2024·2024-03-27

    Smiths Medical Pneupac paraPAC plus 310 ventilators recalled for malfunction

    Smiths Medical is recalling paraPAC plus 310 ventilators that may malfunction by delivering continuous gas flow instead of cycling breaths. The defect affects 10,140 units distributed worldwide and prevents proper ventilation.

    Product
    smiths medical Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP, REF P310NUS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1074-2024·2024-03-27

    Dole Cajun Ranch Chopped Kit Recalled for Potential Listeria Contamination

    Dole Fresh Vegetables is recalling 50,645 cases of Dole Cajun Ranch Chopped Kit UPC 71430002063 due to potential Listeria monocytogenes contamination. The affected product was distributed in 24 U.S. states and Canada.

    Product
    Dole Cajun Ranch Chopped Kit UPC 71430002063
    Category
    Food
    Distribution
    25 states
  • SevereFDA (Devices)·Z-1301-2024·2024-03-27

    HeartMate 3 Left Ventricular Assist System recalled for outflow graft obstruction

    The FDA is recalling the HeartMate 3 Left Ventricular Assist System due to observed outflow graft deformation that can obstruct blood flow. Patients with implanted devices should contact their healthcare provider.

    Product
    HeartMate 3 Left Ventricular Assist System (LVAS): 1. HeartMate 3 Sealed Outflow Graft with Bend Relief, Investigational Device Exemption (IDE) 2. HeartMate 3 Sealed Outflow Graft with Bend Relief, US 3. HeartMate 3 Sealed Outflow Graft with Bend Relief, OUS 4. HeartMate 3 LV
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1080-2024·2024-03-27

    Jack & Olive Ham Torta Sandwich Recalled for Listeria Contamination

    Fresh & Ready Foods LLC recalls Jack & Olive Ham Torta Sandwich due to Listeria monocytogenes contamination. The product was distributed in California, Nevada, Utah, and Arizona with use-by dates from January 27, 2024 to February 15, 2024.

    Product
    Jack & Olive Ham Torta Sandwich on Telera Roll 9 oz UPC 8290690725
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1088-2024·2024-03-27

    HEB Cilantro Cotija Dressing recalled due to Listeria contamination

    Reser's Fine Foods is recalling HEB Cilantro Cotija Dressing due to potential Listeria monocytogenes contamination. The dressing was distributed across multiple states in approximately 5,589 cases.

    Product
    FCF Item 403949, HEB Cilantro Cotija Dressing Perfect for Tacos, 12oz glass bottle, 6 bottles per case. UPC on bottle: 41220 94799.
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Devices)·Z-1275-2024·2024-03-27

    Smiths Medical Pneupac Plus 300 Ventilator Cycling Malfunction

    Smiths Medical Pneupac Plus 300 ventilators may intermittently deliver continuous airflow instead of cycling breaths as designed. This malfunction affects 2,902 units distributed worldwide.

    Product
    smiths medical Pneupac paraPAC plus 300 ventilator kit without PEEP and CPAP, REF P300NUS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1267-2024·2024-03-27

    ARROW QuickFlash Radial Artery Catheters Recalled for Defective Component

    ARROW International is recalling 1,160,470 QuickFlash radial artery catheterization devices due to a defective guidewire handle that can cause arterial vasospasm and vessel injury.

    Product
    ARROW QuickFlash Radial Artery Catherization (wire, guide, catheter), Part Numbers: a) REF AK-04220; b) REF ASK-04220-FMH1; c) REF ASK-04220-HHC; d) REF ASK-04220-KSP; e) REF ASK-04220-PSU; f) REF ASK-04220-UCL1; g) REF ASK-04500-AH; h) REF ASK-04500-HF-S; i) R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1091-2024·2024-03-27

    Chicken Taco Kits Recalled for Listeria Contamination Risk

    Reser's Fine Foods is recalling multiple chicken taco kits distributed across 16 states due to potential Listeria monocytogenes contamination in a repackaged cheese ingredient. Consumers should not consume affected products.

    Product
    Item 404764, KIT EM CHICKEN STREET TACO DP EXPRESS MEAL 6/22 OZ, UPC 7111712500. The following Taco Kits were distributed to consignees with instructions for assembly at retail store kitchen: Item 406987, KIT OP CHICKEN TACO MINI SINGLE SERVE ON PREMISE NO TRAYS 2/2.4925 LB, UP
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Devices)·Z-1300-2024·2024-03-27

    FDA Recalls HeartMate II Left Ventricular Assist Systems for Graft Obstruction

    Thoratec Corp. recalls HeartMate II left ventricular assist system kits due to outflow graft deformation that could obstruct blood flow. The FDA has classified this as a Class I recall affecting 2,240 units distributed worldwide.

    Product
    HeartMate II Left Ventricular Assist System (LVAS): 1. HeartMate II Sealed Outflow Graft with Bend Relief REF 103393 2. HeartMate II LVAS Implant Kit, US REF 106015 3. HeartMate II LVAS Implant Kit, OUS REF 106016 Update (February 14, 2024) HeartMate II Left Ventricular As
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalCPSC·24169·2024-03-21

    Happiness USA Roller Ball Candy Recalled Due to Choking Hazard

    Twenty Four Six Foods LLC is recalling all flavors of Happiness USA Liquid Rolling Candy because the rolling ball applicator can dislodge into a child's mouth, posing a choking hazard and risk of death.

    Product
    Happiness USA Liquid Rolling Candy
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24171·2024-03-21

    Starbucks-branded metallic mugs recalled due to burn and laceration hazards

    Nestlé USA recalls about 440,500 metallic mugs from 2023 holiday Starbucks gift sets sold at Target, Walmart, and military retailers. The mugs can overheat or break when microwaved or filled with extremely hot liquid, causing severe burns and cuts. 10 people have been injured in 12 reported incidents.

    Product
    Metallic Mugs included in 2023 Holiday Starbucks-branded Gift Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1055-2024·2024-03-20

    CK Turkey and Cheese Sandwich recalled for undeclared sesame allergen

    CK Turkey and Cheese Sandwich is recalled for undeclared sesame allergen. The sandwich label lists only Wheat, Milk, and Soy allergens, missing sesame which poses risk to allergic consumers.

    Product
    CK Turkey and Cheese Sandwich, net wt. 6.7oz. Product is closed-face sandwich and ready to eat product. UPC 983644000141. The sandwich label declares "Ingredients: Multigrain Bread ***Contains: Wheat, Milk, Soy."
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1070-2024·2024-03-20

    Trader Joe's Elote Chopped Salad Kit Recalled for Listeria Contamination

    Trader Joe's Company is recalling approximately 7,348 cases of Trader Joe's Elote Chopped Salad Kit nationwide due to potential Listeria monocytogenes contamination. All products with "Used By" dates on or before February 18, 2024 are affected.

    Product
    Trader Joe s Elote Chopped Salad Kit (SKU 74768) 11.94 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1071-2024·2024-03-20

    Trader Joe's Southwest Salad Recalled Due to Listeria Monocytogenes Contamination

    Trader Joe's Company is recalling Trader Joe's Southwest Salad (SKU 56077), 9 oz. due to potential Listeria monocytogenes contamination. Approximately 800,955 units were distributed nationwide.

    Product
    Trader Joe s Southwest Salad (SKU 56077) 9 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1284-2024·2024-03-20

    Vascular guide catheter recalled due to distal end fracture risk

    Medos is recalling CERENOVUS CEREBASE DA Guide Sheaths due to reports of fractures at the distal end. Fractures may delay surgical procedures or cause vascular injury.

    Product
    CERENOVUS CEREBASE DA Guide Sheath, Part Numbers: a) GS9080SD; b) GS9090SD; c) GS9095SD; Vascular guide-catheter, single-use
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-1069-2024·2024-03-20

    Trader Joe's Cilantro Salad Dressing Recalled for Listeria Contamination

    Trader Joe's is recalling Cilantro Salad Dressing (SKU 36420) due to possible Listeria monocytogenes contamination. Approximately 15,890 cases were distributed nationwide.

    Product
    Trader Joe s Cilantro Salad Dressing (SKU 36420) Perishable Keep Refrigerated 12 FL OZ (355mL)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1065-2024·2024-03-20

    BrightFarms Southwest Chipotle Salad Kits Recalled for Listeria Contamination

    BrightFarms Southwest Chipotle Salad Kits are being recalled for potential Listeria monocytogenes contamination in the cotija cheese ingredient. Affected products have best-by dates from December 31, 2023 through February 22, 2024.

    Product
    BrightFarms Southwest Chipotle Salad Kit Ready to eat salad kit containing green lettuce (grown by indoors at BrightFarms) and a master pack supplied by Latitude 36 Foods, which contain cotija cheese, dressing and toppings. Intended for retail distribution to consumers. Cotija
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1056-2024·2024-03-20

    Food recall: Jacksons sandwich with undeclared sesame allergen

    Capitol Commissary LLC recalled 1,382 units of Jacksons Turkey and Cheese Sandwich due to undeclared sesame. The product was distributed across seven Western states and may pose a risk to consumers with sesame allergies.

    Product
    Jacksons Turkey and Cheese Sandwich, net wt. 6.7oz. Product is closed-face sandwich and ready to eat product. UPC 983642601562. The sandwich label declares "Ingredients: Multigrain Bread ***Contains: Wheat, Milk, Soy."
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1035-2024·2024-03-13

    Frios Gourmet Pops Frozen Popsicles Recalled for Undeclared Egg Allergen

    Frios Gourmet Pops frozen popsicles are being recalled because they contain undeclared egg, an allergen. Consumers with egg allergies may face allergic reactions if they consume these products.

    Product
    Frios Gourmet Pops - Banana Pudding Popsicle 3oz frozen popsicle packaged individually in clear plastic sleeve. 48 popsicles per box. *Sold directly to end consumer via food truck
    Category
    Food
    Distribution
    17 states
  • CriticalFDA (Food)·F-1044-2024·2024-03-13

    Vegetarian Pia Cake Taro Durian Recalled for Undeclared Egg Allergen

    LQNN Inc. is recalling Vegetarian Pia Cake Taro Durian (14 oz bags) due to undeclared egg allergen. The recall affects approximately 222,320 bags distributed across 31 U.S. states and Canada.

    Product
    Vegetarian Pia Cake Taro Durian, 14 oz (400g)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1050-2024·2024-03-13

    Vegetarian Pia Cake Recalled for Undeclared Egg Allergen

    LQNN Inc. is recalling 222,320 bags of Vegetarian Pia Cake Mung Bean Pineapple for containing undeclared egg. The product was distributed across 31 U.S. states and Canada.

    Product
    Vegetarian Pia Cake Mung Bean Pineapple, 14oz (400g)
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1047-2024·2024-03-13

    FDA recalls Banh Pia Classic Hopia for undeclared egg allergen

    LQNN Inc. is recalling Banh Pia Classic Hopia because it contains undeclared egg allergen, which can cause serious allergic reactions. About 222,320 bags were distributed across 31 U.S. states and Canada.

    Product
    Banh Pia Classic Hopia, Mung Bean Durian, 16.8oz (480g)
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1053-2024·2024-03-13

    BANH PIA Pumpkin Pia Cake Recalled for Undeclared Egg Allergen

    BANH PIA Liu Sha Pumpkin Pia Cake is recalled because it contains egg that is not declared on the label. The recall affects 222,320 bags distributed across 31 US states and Canada. Consumers with egg allergies should not consume this product.

    Product
    BANH PIA Liu Sha Pumpkin Pia Cake, 480g
    Category
    Food
    Distribution
    0 states