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.

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1726–1750 of 30633

  • HighFDA (Devices)·Z-1539-2026·2026-03-18

    [pending] GEM Premier 5000; Model No. 00055430010.

    Pending LLM rewrite. Source: FDA_DEVICE Z-1539-2026.

    Product
    GEM Premier 5000; Model No. 00055430010.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1538-2026·2026-03-18

    [pending] GEM Premier 5000; Part No. 00055430008.

    Pending LLM rewrite. Source: FDA_DEVICE Z-1538-2026.

    Product
    GEM Premier 5000; Part No. 00055430008.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0551-2026·2026-03-18

    Frozen Blueberry Crumble Pie Recalled for Listeria Risk

    Willamette Valley Pie Company is recalling Frozen Raw Bulk 9 inch Blueberry Crumble Pie due to potential contamination with listeria monocytogenes. The frozen pies were sold to grocery retailers' in-store bakeries in Illinois and Oregon.

    Product
    Frozen Raw Bulk 9 inch Blueberry Crumble Pie ES (4 pies/case). Net wt. 38oz. UPC 00022518893257. Handmade - Willamette Valley Pie Company LLC. 1651 Eska Way, Silverton, OR. Frozen raw pies were sold frozen in bulk packaging to grocery retailers' in-store bakeries. They are inte
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·H-0554-2026·2026-03-18

    Coco's Italian Market Cannoli Making Kit Missing Allergen Declarations

    Coco's Italian Market Cannoli Making Kit is recalled because the label lists flour and ricotta cheese as sub-ingredients but fails to declare wheat and milk allergens. Consumers with wheat or milk allergies may be at risk if they consume the product.

    Product
    Coco's Italian Market Cannoli Making Kit with 6 Cannoli Shells & Cream, Net Wt. 8 oz. (227g), Keep Frozen, packaged in a plastic container, UPC 0680334992716
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0550-2026·2026-03-18

    Frozen Raw Blueberry Crumble Pie Recalled for Listeria Risk

    Willamette Valley Pie Company is recalling frozen raw blueberry crumble pies due to potential listeria monocytogenes contamination. The pies were distributed to grocery store in-store bakeries in Illinois and Oregon.

    Product
    Frozen Raw Bulk 8 inch Blueberry Crumble Pie (4 pies/case). Net wt. 24.5oz. UPC 0002251881223. Handmade - Willamette Valley Pie Company LLC. 1651 Eska Way, Silverton, OR. Frozen Raw pies were sold frozen in bulk packaging to grocery retailers' in-store bakeries. They are intende
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·H-0614-2026·2026-03-18

    CNC Noodle Corporation Fresh Noodles Recall for Undeclared Allergens

    CNC Noodle Corporation is recalling ZHONG HUA CHAO MIAN fresh noodles due to undeclared wheat and Yellow #6 food coloring on the label. Consumers with wheat allergies or sensitivities to the colorant may be at risk.

    Product
    Secondary Packaging: ZHONG HUA CHAO MIAN NOODLE INGREDIENTS: ENRICHED FLOUR, WATER, STARCH, SALT, POTASSIUM, CARBONATE AND BENZOATE OF SODA ADDED AS PRESERVATIVE F.D. & C. YELLOW COLOR #5 & #5 (TARTRAZINE) ARTIFICIAL COLORS) Primary Packaging: CHINA NOODLE CO. FRESH NOODLE NET W
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1534-2026·2026-03-18

    [pending] GEM Premier 5000; Part No. 00055415008.

    Pending LLM rewrite. Source: FDA_DEVICE Z-1534-2026.

    Product
    GEM Premier 5000; Part No. 00055415008.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0621-2026·2026-03-18

    House of Flavors Vanilla Ice Cream Recalled for Undeclared Egg

    House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream (3 gallon tubs) is being recalled because it contains undeclared egg, a common allergen. The recall affects 4,880 tubs distributed in Illinois.

    Product
    House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream, 3 GAL tub
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1503-2026·2026-03-18

    [pending] Penner Pacific Bathing Spa, Model Numbers 360030-1C, 360030-1CE, 360030-1CTS, 360030-XCE, 360030-XC,

    Pending LLM rewrite. Source: FDA_DEVICE Z-1503-2026.

    Product
    Penner Pacific Bathing Spa, Model Numbers 360030-1C, 360030-1CE, 360030-1CTS, 360030-XCE, 360030-XC, 360030-1CT, 360030-1C, 360030-XC, 360030-XCT, 360030-1CTS, 360030-XCTS, 3600301-CTS, 360030-XCE, 360030-1CT, 360030-1CE, 36030-XCT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0553-2026·2026-03-18

    Coco's Italian Market Fettuccini Alfredo recalled for undeclared wheat

    Coco's Italian Market Heat-n-Eat Fettuccini Alfredo is recalled because the label lists semolina and durum flour as sub-ingredients but does not declare wheat. Consumers with wheat allergies or sensitivities may be at risk.

    Product
    Coco's Italian Market Heat-n-Eat Fettuccini Alfredo in homemade Alfredo Sauce, Net Wt. 19 oz. (510g), Keep Frozen, packaged in a microwaveable plastic container, UPC 0680334993607
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1552-2026·2026-03-18

    [pending] DxC 700 AU, REF: B86444, B86446

    Pending LLM rewrite. Source: FDA_DEVICE Z-1552-2026.

    Product
    DxC 700 AU, REF: B86444, B86446
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1544-2026·2026-03-18

    [pending] PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016

    Pending LLM rewrite. Source: FDA_DEVICE Z-1544-2026.

    Product
    PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code: 00721902629013 Catalog Number: 11101-000017 UDI-DI code: 00721902682483 Infant/Child Reduced Energy Defibrillation Electrodes are pre gelled, self-adhesive, the
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1549-2026·2026-03-18

    [pending] Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16

    Pending LLM rewrite. Source: FDA_DEVICE Z-1549-2026.

    Product
    Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1542-2026·2026-03-18

    [pending] GEM Premier 5000; Part No. 00055445008.

    Pending LLM rewrite. Source: FDA_DEVICE Z-1542-2026.

    Product
    GEM Premier 5000; Part No. 00055445008.
    Category
    Medical Device
    Distribution
    Distributed nationwide