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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13376–13400 of 27735

  • CriticalFDA (Food)·F-1082-2024·2024-03-27

    Stonewall Kitchen Gluten Free Doughnut Mix Recalled for Undeclared Wheat

    Stonewall Kitchen is recalling Cinnamon Sugar Doughnut Mix (Gluten Free) with use-by dates of March 9-10, 2025, because units contain undeclared wheat. Consumers with wheat allergies or celiac disease should not consume this product.

    Product
    Stonewall Kitchen Cinnamon Sugar Doughnut Mix; Gluten Free; Home-Baked & Gluten Free; Net Wt. 18oz (510g); UPC: 1138131332
    Category
    Food
    Distribution
    44 states
  • CriticalFDA (Food)·F-1087-2024·2024-03-27

    Don Pancho Fiesta Sauces Recalled for Listeria Monocytogenes Contamination

    Reser's Fine Foods is recalling Don Pancho Fiesta 3 Pack Everything Sauce due to potential Listeria monocytogenes contamination from recalled Cotija cheese repackaged into these ready-to-eat products.

    Product
    Item # 407034, Don Pancho Fiesta 3 Pack Everything Sauce. Each pack consists of Cilantro Lime Crema, Baja-Style Crema, Chipotle Crema. 3/12oz glass bottles per pack, 6 packs per case. UPC on 3-pack box: 0 71117 00741 1.
    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 (Food)·F-1072-2024·2024-03-27

    Dole Chopped Kit Avocado Ranch Recalled for Potential Listeria Contamination

    Dole Chopped Kit Avocado Ranch (UPC 71430000915) is being recalled due to potential contamination with Listeria monocytogenes. The FDA Class I recall affects 50,645 cases distributed across the United States and Canada.

    Product
    Dole Chopped Kit Avocado Ranch UPC 71430000915
    Category
    Food
    Distribution
    25 states
  • SevereFDA (Drugs)·D-0393-2024·2024-03-27

    FDA Recalls Unapproved Tianeptine Elixir Drug Product Nationwide

    Neptune's Fix Tianeptine Elixir, distributed nationwide by Super Chill Products, is recalled because it contains tianeptine, a substance not approved by the FDA for any medical use in the United States. Consumers should not use this product.

    Product
    Neptune's Fix, Tianeptine Elixir, Fast Acting, 0.338 fl.oz. (10 mL) bottle, Distributed By Superchill Products, 827 6th Avenue, New York, New York 10001.
    Category
    Drug
    Distribution
    Distributed nationwide
  • 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 (Food)·F-1096-2024·2024-03-27

    Wesco mint no-bake cookie bites recalled for undeclared peanut and soy allergens

    Wesco Central Commissary is recalling Wesco mint no-bake cookie bites because they contain undeclared peanut and soy allergens that are not listed on the label. The affected product was distributed in Michigan.

    Product
    Wesco mint no-bake cookie bites 9oz cup UPC 750308040474
    Category
    Food
    Distribution
    1 state
  • 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-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-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-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-1079-2024·2024-03-27

    Sprig & Sprout Ham Torta Sandwich recalled for Listeria monocytogenes contamination

    Sprig & Sprout Ham Torta Sandwich is being recalled due to potential Listeria monocytogenes contamination. The product was distributed to CA, NV, UT, and AZ with Use By dates from January 27 to February 15, 2024.

    Product
    Sprig & Sprout Ham Torta Sandwich on Telera Roll 9 oz UPC 8290690720
    Category
    Food
    Distribution
    4 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
  • 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 (Food)·F-1086-2024·2024-03-27

    Cilantro Lime Crema Products Recalled for Listeria Contamination

    Reser's Fine Foods is recalling Cilantro Lime Crema products sold under Costco and Don Pancho labels due to Listeria monocytogenes contamination. Products were distributed across 16 states.

    Product
    FCF Item #404967, Costco Item #1506878, Cilantro Lime Crema, 60/4oz plastic cups per case. Labeled cups only sold in bulk for Food Service Use not for individual sale. UPC 13454 38195. FCF Item #404689, Don Pancho Cilantro Lime Crema Everything Sauce, 32oz glass bottle, sold as
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Food)·F-1076-2024·2024-03-27

    Marketside Chopped Salad Kit Recalled for Potential Listeria Contamination

    Dole Fresh Vegetables Inc is recalling Marketside Chopped Salad Kit Bacon Crunch due to potential Listeria monocytogenes contamination. Affected packages have lot codes B020-B036 with production dates from February 5, 2024 through February 21, 2024.

    Product
    Marketside Chopped Salad Kit Bacon Crunch UPC 681131305440
    Category
    Food
    Distribution
    25 states
  • 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-1090-2024·2024-03-27

    Costco Southwest Wrap Kit Recalled for Listeria Contamination

    Reser's Fine Foods is recalling Costco Southwest Wrap Kits due to Listeria monocytogenes contamination. The product was distributed across 16 states.

    Product
    FCF Item 406957, Costco Item # 1744097, Club COSTCO SW Wrap Kit, Costco Service Deli, 2/8.15 lbs. Net Wt. 16.31 lbs., UPC 0 13454 38424 4. Costco assembled and sold product as Southwest Wrap with Sauce, item #29433.
    Category
    Food
    Distribution
    16 states
  • HighFDA (Devices)·Z-1320-2024·2024-03-27

    Medical Device Recall: Orthopedic Compression Screws with Incorrect Dimensions

    In2Bones, SAS is recalling I.B.S Compression screws due to a batch mix-up. Affected screws may have different lengths than indicated on their labels, creating a risk of improper surgical implantation.

    Product
    I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 80mm,Part Number S65 ST180
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1342-2024·2024-03-27

    Surgical Guidewire Introducer Sheath Recalled for Internal Manufacturing Defects

    Angiodynamics vascular guidewire introducers (600 units) may have internal defects preventing proper function during surgery. Defects could cause procedure delays and require device exchange.

    Product
    MINI STICK MAX 4F X 10 CM STIFF .018 NI/TU NON-ECHO 2.75" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-762
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1310-2024·2024-03-27

    ECMO heat exchanger module recalled due to water path restriction

    Mc3 Inc is recalling 188 Nautilus Smart ECMO modules nationwide due to potential water path restrictions in the heat exchanger that may cause inadequate heat transfer and risk of hypothermia during use.

    Product
    NautilusTM Smart ECMO Module with Balance Biosurface-used in extracorporeal life support procedures to oxygenate blood, remove carbon dioxide and regulate blood temperature. Product Number: 48135, 48135E
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1081-2024·2024-03-27

    Bread Butter White Bread Recalled Due to Foreign Material Contamination

    Albertsons is recalling Signature Select, Athens, and Cal Pia brand Bread Butter White Bread due to possible metal and plastic shavings in the product. The recall affects approximately 13,550 units distributed in California and Nevada.

    Product
    Signature Select, Athens, and Cal Pia brand Bread Butter White Bread 22 oz. loaf
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1308-2024·2024-03-27

    Curaplex Nasal Intubation Kit with incompatible tube holder recalled

    Sarnova HC is recalling the Curaplex Nasal Intubation Kit because the endotracheal tube holder is incompatible with nasal intubation, preventing practitioners from securing the tube. The recall affects 550 units distributed nationwide.

    Product
    Curaplex Nasal Intubation Kit w/ 7mm Endotracheal Tube-To perform a nasal intubation to establish an airway in an emergency. Item Number: 023070S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1321-2024·2024-03-27

    Preat Nobel RP Titanium Abutment Blank Recalled for Manufacturing Defect

    Preat Corp is recalling 561 units of RP Titanium Abutment Blanks due to a manufacturing defect where the screw seat location may be too high, resulting in shortened screw engagement into the implant.

    Product
    Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967
    Category
    Medical Device
    Distribution
    Distributed nationwide