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.

Filters

Agency

Category

Minimum severity

Clear filters

17501–17525 of 89825

  • HighFDA (Devices)·Z-2424-2023·2023-08-23

    Endoscopic surgical grasper recalled due to rotation knob defect

    Carefusion is recalling specific lots of Snowden-Pencer Diamond-Touch endoscopic graspers due to a manufacturing defect that may cause the rotation knob to crack or break. Affected units were distributed in the US and Canada.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH GRASPERS CROCODILE GRASPER, DOUBLE ACTI 5MM, 32CM, RATCHETED HANDLE, REF SP90-7066; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1448-2023·2023-08-23

    Frozen Sachertote Recalled for Undeclared Egg, Milk, and Wheat Allergens

    Lidl US TRADING is recalling Alpenfest Style Sachertote frozen dessert because egg, milk, and wheat allergens are not declared on the label. Consumers with allergies to these ingredients should not consume the product.

    Product
    Alpenfest Style Sachertote NET WT 17.6 OZ (1 LB 1.6OZ) 500g Frozen UPC:2010 0889 Packaged in Cardboard Carton.
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-2418-2023·2023-08-23

    Endoscopic Dissector Surgical Tool Recalled for Cracking Knob Defect

    Carefusion 2200 Inc is recalling Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR endoscopic surgical instruments due to potential cracking of the rotation knob from incorrect adhesive use in manufacturing. Lot B23 is affected.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR FENESTRATED 16MM JAW 5MM, 32CM, NON RATCHETED, REF SP90-7036; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1405-2023·2023-08-23

    Dilettante Dark Ephemere Bulk Truffles Milk Allergen Mislabeling

    Dilettante Mocha Cafe Dark Ephemere Bulk Truffles' display placard lists milk in ingredients but declares only 'Contains: Dairy,' not 'Contains: Milk.' Bulk boxes have correct allergen labeling.

    Product
    Dilettante Mocha Cafe brand Dark Ephemere Bulk Truffles, perishable, sold individual pieces out of retail display cases. The display placard declares milk, cream, and butter in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1442-2023·2023-08-23

    Uro Kid Support Capsules recalled due to potential E. coli contamination

    Global Vitality Inc. is recalling Uro Kid Support Capsules due to potential E. coli contamination. The affected product was distributed to a single location in California.

    Product
    Food Research International - Uro Kid Support Capsules, packaged in glass bottle, 90 capsules per bottle, 12 bottles per case
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2417-2023·2023-08-23

    Endoscopic surgical graspers recalled for potential rotation knob cracking

    Carefusion is recalling Snowden-Pencer MIS surgical graspers (lot B23) distributed in the US and Canada because the rotation knob may crack or break due to a manufacturing adhesive defect. Affected devices could malfunction during surgical use.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH ATRAUMATIC GRASPER DIAMOND JAW 5MM, 32CM, RATCHETED, REF SP90-7020; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1429-2023·2023-08-23

    Romaine Lettuce Recalled Due to Potential Deer Feces Contamination

    G.O. Corporation is recalling Romaine Lettuce All American sold in four states due to potential contamination with deer feces.

    Product
    Lettuce Romaine All American, packaged in the following sizes and configurations: 1. Produce Code 476702, 1-5 lb. bag per shipping case, Customer UPC 8398299; 2. Produce Code 476709, 4-5 lb. bags per shipping case, Customer UPC 476709, 8336156, and 8398281.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1423-2023·2023-08-23

    Romaine lettuce recalled due to potential deer feces contamination

    G.O. Corporation is recalling romaine lettuce in multiple package sizes due to potential contamination with deer feces. The affected products were distributed to Iowa, Minnesota, North Dakota, and Wisconsin.

    Product
    Romaine lettuce packaged into the following configurations and sizes: 1. Lettuce Romaine Shred, Produce Code 720325, 4-2.5lb. bags per shipping case, Customer UPC 9120457. 2. Romaine Shred 1/4", Produce Code 720425, 4-2.5lb bags per shipping case, Customer UPC 7641269…
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1427-2023·2023-08-23

    Romaine Lettuce Recalled Due to Deer Feces Contamination

    G.O. Corporation is recalling Romaine Lettuce 80/20 GB due to potential contamination with deer feces. The affected products were distributed to Iowa, Minnesota, North Dakota, and Wisconsin.

    Product
    Lettuce Romaine 80/20 GB, packaged in the following sizes and configurations: 1. Produce Code 448007, 2-5 lb. bags per shipping case, 2. Produce Code 448007, 4-5 lb. bags per shipping case, 3. Produce Code 448110, 4-5 lb. bags per shipping case.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1402-2023·2023-08-23

    Trader Joe's Falafel Recalled for Foreign Object Contamination

    Trader Joe's Fully Cooked Falafel Heat & Eat is being recalled from Connecticut, Texas, and Illinois due to the presence of rocks in the product. Consumers should return affected packages to the point of purchase.

    Product
    Trader Joe's Fully Cooked Falafel Heat & Eat NET WT. 12 OZ (340g) Distributed and Sold Exclusively By: Trader Joe's Monrovia, CA 91016 UPC 0093 9355
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1410-2023·2023-08-23

    Dilettante Mocha Cafe Amaretto Bulk Truffle Allergen Labeling Error

    Dilettante Chocolates is recalling Mocha Cafe brand Amaretto Bulk Truffle chocolate sold from retail display cases due to incomplete allergen declaration on the display placard.

    Product
    Dilettante Mocha Cafe brand Amaretto Bulk Truffle, perishable, sold individual pieces out of retail display cases. The display placard declares milk chocolate and almond extract in the ingredients statement, but the Contains statement declares "Contains: Dairy, Nuts". Bulk…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2413-2023·2023-08-23

    HF Resection Electrodes Recalled for Wire Breakage and Patient Fragment Hazard

    Olympus HF Resection Electrodes are being recalled due to reports of loop wire breakage when contacting metal objects. Broken fragments can fall inside the patient and require retrieval.

    Product
    HF Resection Electrodes - HF resection electrodes are part of a resectoscope system for endoscopic diagnosis and treatment in urological or gynecological applications. 64 Models: 1) A22201C 2) A22201D 3) A22202C 4) A22203C 5) A22205C 6) A22205D 7) A22206C 8)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1437-2023·2023-08-23

    Pumpkin Creme Cookies Recalled Due to Undeclared Peanut Allergen

    Commercial Bakeries is recalling Ruxton Chocolates Manning Brand Pumpkin Creme Cookies because the product contains undeclared peanut. The recall affects 4834 cases distributed to retail locations in IL, NJ, MD, NY, CT, CA, and FL.

    Product
    Ruxton Chocolates Manning Brand Pumpkin Creme Cookies 19.5 oz. Bulk product packaged in bags, 12 bags per case.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-2429-2023·2023-08-23

    Snowden-Pencer Surgical Dissector Rotation Knob May Crack or Break

    Carefusion 2200 Inc is recalling specific lots of the Snowden-Pencer MIS surgical dissector because the rotation knob may crack or break due to a manufacturing defect.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR DIAMOND JAW 5MM, 45CM, RATCHETED, REF SP90-7271; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1425-2023·2023-08-23

    Romaine lettuce blend recalled for potential fecal contamination

    G.O. Corporation is recalling a lettuce blend product due to potential contamination with deer feces. Affected products were distributed in Iowa, Minnesota, North Dakota, and Wisconsin.

    Product
    Lett. Blend Rom/End/Rad-All Seasons packaged in the following sizes and configurations: 1. Produce Code 444032, 6-2 lb. bags per shipping case 2. Produce Code 444047, 3-2lb. bags per shipping case.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-2428-2023·2023-08-23

    Endoscopic Surgical Grasper Recalled for Potential Rotation Knob Cracking

    Carefusion is recalling specific lots of surgical graspers due to potential cracking of the rotation knob caused by incorrect adhesive use in manufacturing. Affected devices may fail during surgical procedures.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH GRASPERS CROCODILE GRASPER, DOUBLE ACTI 5MM, 45CM, RATCHETED HANDLE, REF SP90-7266; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1426-2023·2023-08-23

    Romaine Lettuce Mix Recalled for Potential Deer Feces Contamination

    G.O. Corporation is recalling lettuce mix containing romaine (Produce Code 421009) due to potential contamination with deer feces. The affected products were distributed in Iowa, Minnesota, North Dakota, and Wisconsin.

    Product
    Lettuce Mix w 20 Romaine, Produce Code 421009, 4-5 lb. bags per shipping case,
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-2425-2023·2023-08-23

    Endoscopic Surgical Dissectors Recalled for Potential Rotation Knob Cracking

    Carefusion 2200 Inc recalls 42 units of Snowden-Pencer surgical dissectors distributed in the US and Canada due to potential cracking of the rotation knob caused by an adhesive defect in manufacturing.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR DIAMOND JAW 5MM, 32CM, RATCHETED, REF SP90-7071; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1428-2023·2023-08-23

    Lettuce Rom Blend recalled due to potential deer feces contamination

    G.O. Corporation is recalling Lettuce Rom Blend (23,186 lbs.) distributed to IA, MN, ND, and WI because the lettuce may be contaminated with deer feces.

    Product
    Lettuce Rom Blend 50/50, packaged in the following sizes and configurations: 1. Produce Code 448909, 4-5 lb. bags per shipping case, Customer UPC 3127222; 2. Produce Code 449007, 2-5 lb. bags per shipping case, Customer UPC 6862312; 3. Produce Code 449009, 4-5 lb.…
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1408-2023·2023-08-23

    Dilettante Mocha Cafe Champagne Truffles recalled for milk allergen labeling discrepancy

    Dilettante Mocha Cafe Champagne Bulk Truffles are being recalled due to milk allergen labeling errors on display case placards in Washington. The allergen declaration does not adequately reflect milk content.

    Product
    Dilettante Mocha Cafe brand Champagne Bulk Truffles, perishable, sold individual pieces out of retail display cases. The display placard declares milk in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sent to retail stores…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-1084-2023·2023-08-23

    Toothpaste Label Mix-Up: Wrong Tube Labels in Strawberry Cartons

    Hello wild strawberry fluoride toothpaste cartons contain tubes incorrectly labeled as hello fresh watermelon fluoride free toothpaste. 182,046 units affected nationwide.

    Product
    hello wild strawberry fluoride toothpaste, sodium fluoride 0.24% (0.15% w/v fluoride ion), NET WT 4.2 OZ (119 g), Distributed by Hello Products LLC, Montclair, NJ 07042, UPC 8 19156 02026 4 (carton), 12-count case GTIN: 20819156020268; strawberry tubes also sold in Strawberry…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1406-2023·2023-08-23

    Dilettante Mocha Cafe Truffles recalled for incomplete milk allergen labeling

    Dilettante Chocolates Inc is recalling Mocha Cafe brand Light Ephemere Bulk Truffles sold from retail display cases in Washington due to incomplete allergen labeling on the display placard.

    Product
    Dilettante Mocha Cafe brand Light Ephemere Bulk Truffles, perishable, sold in individual pieces out of retail display cases. The display placard declares cream and butter in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2423-2023·2023-08-23

    Surgical grasper recalled for rotation knob cracking due to adhesive defect

    Carefusion is recalling Snowden-Pencer endoscopic graspers due to potential rotation knob cracking from a manufacturing adhesive defect. Affected lot B23 was distributed in the US and Canada.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH GRASPER CRILE CURVED JAW 5MM, 32CM, RATCHETED, REF SP90-7048; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1459-2023·2023-08-23

    IO Inspired Organics Walnut Halves & Pieces recalled for undeclared walnuts

    IO Inspired Organics Walnut Halves & Pieces are recalled because walnuts are not declared in the ingredient and contains statement. The 7oz packages were distributed in 11 states and may pose a risk to consumers with walnut allergies.

    Product
    IO Inspired Organics brand Organic Raw Walnut Halves & Pieces; 7oz plastic tubs; 9 packages per wholesale case; retail UPC 863669740065, Lipari #943469
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-1416-2023·2023-08-23

    Dilettante Mocha Cafe Toffee Recalled for Incomplete Allergen Labeling

    Dilettante Chocolates recalls Rheingold White Bulk Toffee sold at Washington retail locations due to display placard with incomplete allergen declarations. The placard did not fully identify milk and specific nut allergens present in the product.

    Product
    Dilettante Mocha Cafe brand Rheingold White Bulk Toffee, perishable, sold individual pieces out of retail display cases. The display placard declares milk, pecans and hazelnuts in the first Contains statement, and the 2nd Contains statement declares "Contains: Dairy, Nuts".…
    Category
    Food
    Distribution
    1 state