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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1426–1450 of 26027

  • SevereFDA (Food)·H-0563-2026·2026-03-18

    Made Fresh Salads Strawberry Cream Cheese recalled for Listeria contamination

    Made Fresh Salads brand Strawberry Cream Cheese in 5 lb tubs is being recalled due to potential Listeria monocytogenes contamination. The product was distributed in New York.

    Product
    Made Fresh Salads brand Strawberry Cream Cheese; 5 lb white plastic tub
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·H-0546-2026·2026-03-18

    Rosabella Brand Moringa Dietary Supplement Capsules Contaminated with Salmonella

    Ambrosia Brands LLC is recalling Rosabella brand Moringa dietary supplement capsules nationwide and internationally because the product may be contaminated with Salmonella.

    Product
    Rosabella brand MORINGA; DIETARY SUPPLEMENT CAPSULES; 60 capsules per bottle; Distributed by: Ambrosia Brands, LLC, 625 Randall Ave, St. 100, Cheyenne, WY 82001; SUGGESTED USE: As a dietary supplement, take two (2) veggie capsules once a day. For best results, take 20-30 min befo
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1546-2026·2026-03-18

    Blood Glucose Meter Instructions Inadequately Label Critical E-5 Error Code

    Trividia Health recalls Owner's Booklets for TRUE METRIX PRO blood glucose meters because labeling inadequately explains the E-5 error code, which can represent very high blood glucose levels. Unclear instructions could delay medical attention when users experience this critical error.

    Product
    Owner's Booklets and Instructions for Use that are used with the following blood glucose measurement devices. Description/Item: TRUE METRIX PRO Meter Only/RE4H01P-40, TRUE METRIX PRO Starter Kit/RE4H01P-43, PROCURE TRUE METRIX PRO Meter Only/RE4212P-00, Henry Schein TRUE MET
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1547-2026·2026-03-18

    Blood glucose monitor instructions inadequately label critical error code E-5

    Instructions for TRUE METRIX AIR blood glucose meters are recalled for inadequately explaining the E-5 error code, which can indicate dangerously high blood sugar. Users may not recognize the need to seek immediate medical attention.

    Product
    Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX AIR Kit/REA4001-01, Leader TRUE METRIX AIR Kit/REA4002-01, CVS TRUE METRIX AIR Kit/REA4007-01, GNP TRUE METRIX AIR Kit/REA4011-
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1548-2026·2026-03-18

    Blood glucose monitor instructions recalled for unclear error code labeling

    Trividia Health is recalling TRUE METRIX GO blood glucose monitor instruction manuals because the labeling fails to clearly explain what an E-5 error code means or when to seek medical help, risking delayed treatment for high blood glucose emergencies.

    Product
    Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX GO Kit/RF4001-01BK, CVS TRUE METRIX GO Kit/RF4007-01, Meijer TRUE METRIX GO Kit/RF4019-01, Fred's Phamarcy TRUE METRIX GO Kit/R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0560-2026·2026-03-18

    Made Fresh Salads Jalapeno Cheddar Cream Cheese Listeria Recall

    Made Fresh Salads brand Jalapeno Cheddar Cream Cheese in 5 lb tubs is recalled due to potential Listeria monocytogenes contamination. The product was distributed in New York.

    Product
    Made Fresh Salads brand Jalapeno Cheddar Cream Cheese; 5 lb white plastic tub
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·H-0561-2026·2026-03-18

    Made Fresh Salads Lox Cream Cheese recalled for Listeria contamination

    Made Fresh Salads brand Lox Cream Cheese (5 lb tubs) is recalled due to potential Listeria monocytogenes contamination. Consumers should not consume affected products.

    Product
    Made Fresh Salads brand Lox Cream Cheese; 5 lb white plastic tub
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·H-0562-2026·2026-03-18

    Made Fresh Salads Scallion Cream Cheese Recalled for Listeria

    Made Fresh Salads brand Scallion Cream Cheese in 5 lb tubs is being recalled because the product may be contaminated with Listeria monocytogenes. All expiration dates through 2/27/2026 are affected.

    Product
    Made Fresh Salads brand Scallion Cream Cheese; 5 lb white plastic tub
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·H-0557-2026·2026-03-18

    Made Fresh Salads Blueberry Cream Cheese Recalled for Listeria Contamination

    Made Fresh Salads brand Blueberry Cream Cheese (5 lb tubs) sold in New York is being recalled due to potential contamination with Listeria monocytogenes. The FDA classifies this as a Class I recall.

    Product
    Made Fresh Salads brand Blueberry Cream Cheese; 5 lb white plastic tub
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·H-0558-2026·2026-03-18

    Made Fresh Salads Garlic Herb Cream Cheese Recalled for Listeria

    Made Fresh Salads brand Garlic & Herb Cream Cheese (5 lb tubs) is being recalled because it may be contaminated with Listeria monocytogenes. The affected product was distributed in New York.

    Product
    Made Fresh Salads brand Garlic & Herb Cream Cheese; 5 lb white plastic tub
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·H-0565-2026·2026-03-18

    Made Fresh Salads Vegetable Cream Cheese Recalled for Listeria

    Made Fresh Salads brand Vegetable Cream Cheese in 5 lb tubs is being recalled due to potential Listeria monocytogenes contamination. Affected products have expiration dates through February 27, 2026.

    Product
    Made Fresh Salads brand Vegetable Cream Cheese; 5 lb white plastic tub
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·H-0555-2026·2026-03-18

    Made Fresh Salads Apple Cinnamon Cream Cheese recalled for Listeria

    Made Fresh Salads brand Apple Cinnamon Cream Cheese in 5 lb tubs is being recalled because the product may be contaminated with Listeria monocytogenes. The recall affects products distributed in New York with all expiration dates through 2/27/2026.

    Product
    Made Fresh Salads brand Apple Cinnamon Cream Cheese; 5 lb white plastic tub
    Category
    Food
    Distribution
    0 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-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 (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 (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 (Drugs)·D-0400-2026·2026-03-18

    Icosapent Ethyl Prescription Capsules Recalled for Oxidized Active Ingredient and Melted Capsules

    Zydus Pharmaceuticals is recalling approximately 60,541 bottles of Icosapent Ethyl 1-gram capsules nationwide due to capsule defects, including melted capsules and red dots caused by oxidized active ingredient. No illnesses have been reported.

    Product
    ICOSAPENT ETHYL — ICOSAPENT ETHYL (ICOSAPENT ETHYL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1512-2026·2026-03-18

    Waldemar Link Endo-Model Replacement Plateau Implant Bushing Detachment Risk

    Waldemar Link is recalling Endo-Model Replacement Plateau implants due to risk that the bushing could detach from the screw shaft due to longitudinal fracture.

    Product
    Endo-Model Replacement Plateau; Item Number: 15-0027/15;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1515-2026·2026-03-18

    Endo-Model Replacement Plateau Screw Bushing Could Detach During Use

    Waldemar Link is recalling Endo-Model Replacement Plateau surgical implants due to potential bushing detachment from the screw shaft. The defect could cause implant failure.

    Product
    Endo-Model Replacement Plateau; Item Number: 15-2835/12;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1521-2026·2026-03-18

    Endo-Model Replacement Plateau orthopedic implant: bushing detachment risk

    Waldemar Link is recalling Endo-Model Replacement Plateau implants due to the potential for bushing detachment from the screw shaft caused by longitudinal fracture. Affected units were distributed in the US and worldwide.

    Product
    Endo-Model Replacement Plateau; Item Number: 15-0027/11;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1524-2026·2026-03-18

    GEM Premier 5000 PAK Cartridges Recalled for Increased Ejection Failures

    Instrumentation Laboratory is recalling GEM Premier 5000 PAK cartridges due to an increased incidence of cartridge ejection errors during device warm-up, which may delay lab result turnaround times.

    Product
    GEM Premier 5000 PAK, Part No. 00055360004.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1553-2026·2026-03-18

    Chemistry Analyzer Software Defect Disables System and Delays Diagnosis

    Beckman Coulter's Chemistry Analyzer AU5800 may fail when the calibration monitor is open beyond 15 minutes, halting patient analysis and potentially delaying diagnosis.

    Product
    CHEMISTRY ANALYZER AU5800, REF: B96697, B96698, B23279, B23280, B23281
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1511-2026·2026-03-18

    Orthopedic implant connection component recalled due to potential bushing detachment

    Waldemar Link is recalling Endo-Model SL Connection Component implants due to potential bushing detachment from the plateau screw caused by longitudinal fracture. 44 units affected worldwide.

    Product
    Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/05;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1498-2026·2026-03-18

    Raz Mobile Shower Commode Chair Seat Brackets May Fail to Properly Engage

    Raz mobile shower commode chair seats may not be properly secured due to vendor modifications that can cause rear seat brackets to fail to engage, creating instability risk for mobility-impaired users.

    Product
    Raz-AT (Attendant Tilt) Mobile Shower Commode Chair, Catalog Number Z300 UDI-DI code: (01)00628758003007 Raz-ART (Attendant Rotational Tilt) Mobile Shower Commode Chair, Catalog Number Z333 UDI-DI code: (01)00628758003335 Raz-AT600 (Bariatric Tilt) Mobile Shower Commode C
    Category
    Medical Device
    Distribution
    Distributed nationwide