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

19226–19250 of 90006

  • HighNHTSA·23V395000·2023-06-01

    Altec aerial device trucks: forward collision braking system software miscalibration

    Altec is recalling 2020-2023 aerial device trucks due to collision mitigation system software that may not be calibrated correctly, preventing the active braking system from activating. This increases the risk of a crash.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V394000·2023-06-01

    2022-2023 Land Rover Range Rover Rear Taillight Link Defect Recall

    Land Rover is recalling 2022-2023 Range Rovers because a damaged rear taillight link can cause exterior lights to fail, reducing visibility and increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V392000·2023-06-01

    2023 Subaru Ascent Front Lower Control Arm Separation Recall

    2023 Subaru Ascent vehicles may have improperly tightened ball joint castle nuts in the lower control arm, risking separation and loss of vehicle control. Free replacement at dealers.

    Product
    SUBARU — SUBARU ASCENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V390000·2023-06-01

    2020-2021 Jayco Melbourne Motorhomes Recalled for Instrument Cluster Failure

    Jayco is recalling certain 2020-2021 Melbourne motorhomes because the instrument cluster may fail and display nothing. Drivers would lose access to critical vehicle information, increasing crash risk.

    Product
    JAYCO — JAYCO MELBOURNE PRESTIGE, MELBOURNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0925-2023·2023-05-31

    Lay's Potato Chips Recalled for Undeclared Milk Allergen

    Frito-Lay is recalling Lay's Classic Potato Chips due to undeclared milk. The recall affects specific products distributed in Connecticut, Massachusetts, Maine, and New Hampshire.

    Product
    Lay s Classic Party Size Potato Chips 13 oz. (368.5 g) UPC 028400310413 packaged in a yellow flexible bag and Lay s Classic Mix and Match Potato Chips 15 5/8 oz (442.9 g) UPC 0028400720151 packaged in a yellow flexible bag
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Devices)·Z-1618-2023·2023-05-31

    Pediatric Ventricular Assist Device Blood Pumps Recalled for Potential Membrane Disruption

    BERLIN HEART GMBH recalls EXCOR Pediatric Ventricular Assist Device Blood Pumps due to potential disruption in triple-layer membranes. The 335 affected units were distributed to multiple US states and Canada.

    Product
    EXCOR Pediatric Ventricular Assist Device Blood Pumps, Models: P10P-001 (10 ml blood pump); P15P-001 (10 ml blood pump); P25P-001x01 (25 ml blood pump); P30P-001x01 (30 ml blood pump), P50P-001 (50 ml blood pump); P60P-001 (60 ml blood pump). Recall occurred in 2018, and was…
    Category
    Medical Device
    Distribution
    16 states
  • SevereFDA (Food)·F-0929-2023·2023-05-31

    Washington Crab Crabcakes Recalled Due to Undeclared Allergens

    Washington Crab & Seafood Company recalls crabcakes due to undeclared allergens: egg, wheat, and soy. The product was distributed to North Carolina and South Carolina.

    Product
    CRABCAKE Ingredients: Blue Crabmeat, mayonnaise, onion bread crumbs, egg solids, salt, spices paprika WASHINGTON CRAB Carolina seafood
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0924-2023·2023-05-31

    Lancaster Spinach Recalled for Possible Listeria Contamination

    Lancaster Spinach, 10-ounce packages, is recalled due to possible contamination with Listeria monocytogenes. Products were distributed in Massachusetts, Maryland, Pennsylvania, New York, New Jersey, and Virginia.

    Product
    LANCASTER SPINACH, 10 OZ, UPC:8-13055-01145-3. Packaged in sealed plastic bags, 12 in a case.
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-1594-2023·2023-05-31

    COVID-19 At-Home Test Kits Recalled for Bacterial Buffer Contamination

    SD Biosensor is recalling 2,712,767 Pilot COVID-19 At-Home Test kits nationwide due to bacterial contamination in the liquid buffer component. Users may notice an odor from affected kits.

    Product
    Pilot COVID-19 At-Home Test, Reference Number 9901-NCOV-10G, Catalog Number 99COV200L-EN02, UPC Code: 887473000207 (EAN-13: 08800111707728)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0921-2023·2023-05-31

    Multiple kale greens products recalled for possible Listeria contamination

    Lancaster Foods LLC is recalling ROBINSON FRESH and LANCASTER kale greens products due to possible Listeria monocytogenes contamination. Affected products have a best-by date of May 1, 2023, and were distributed in MA, MD, PA, NY, NJ, and VA.

    Product
    ROBINSON FRESH KALE GREENS, NET WT 16 OZ, UPC:0-95829-60015. Packaged in sealed plastic bags, 8 in a case. ROBINSON FRESH KALE GREENS NET WT 32 OZ UPC: 0-95829-60016-6. Packaged in sealed plastic bags, 8 in a case. LANCASTER Chopped Kale NET WT 4 OZ CHOPPED KALE. Packaged in…
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0922-2023·2023-05-31

    Giant Curly Leaf Spinach Recalled for Possible Listeria Contamination

    Lancaster Foods LLC is recalling Giant Curly Leaf Spinach due to possible Listeria monocytogenes contamination. The product was distributed in MA, MD, PA, NY, NJ, and VA.

    Product
    GIANT CURLY LEAF SPINACH, 12 /8 OZ, UPC: 6-88267-09813-0. Packaged in sealed plastic bags, 12 in a case.
    Category
    Food
    Distribution
    6 states
  • SevereNHTSA·23V387000·2023-05-31

    Triple E Recalls 2023 Motorhomes Due to LPG Gas Leak Risk

    Triple E is recalling 2023 Unity and Wonder motorhomes because an improperly crimped 2-stage regulator may cause a gas leak, increasing the risk of fire.

    Product
    TRIPLE E RV — TRIPLE E RV, TRIPLE E WONDER, UNITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0923-2023·2023-05-31

    Collard Greens Recalled Due to Possible Listeria Contamination

    Lancaster Foods is recalling Robinson Fresh and Giant collard greens due to possible contamination with Listeria monocytogenes. Affected products distributed in the Northeast and Mid-Atlantic should not be consumed.

    Product
    ROBINSON FRESH COLLARD GREENS, 16 OZ, UPC:0-95829-60006-7. Packaged in sealed plastic bags, 8 in a case. GIANT COLLARD GREENS, 16 OZ, UPC: 6-88267-05311-5. Packaged in sealed plastic bags, 8 in a case.
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0931-2023·2023-05-31

    Tuna Salad Cup Recalled Due to Undeclared Egg Allergen

    Ultra Tuna Salad Cup (DishD'Lish brand) distributed in Washington is recalled because the label does not declare egg as an ingredient. Consumers with egg allergies should not consume this product.

    Product
    Ultra Tuna Salad Cup, brand DishD'Lish, packaged in plastic cup. Label declares Housemade Albacore Tuna Salad, Arugula, Cucumber and Cherry Tomatoes.
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·23V388000·2023-05-31

    Bugatti Recalls One 2023 Chiron Super Sport for Incorrect Wheels

    Bugatti is recalling one 2023 Chiron Super Sport because incorrect wheels were installed, which may cause loss of vehicle control in Top Speed Mode.

    Product
    BUGATTI — BUGATTI CHIRON SUPER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0933-2023·2023-05-31

    House Made Tarragon Chicken Salad Sandwich—undeclared egg and wheat allergens

    FDA recalls House Made Tarragon Chicken Salad Sandwich by DishD'Lish because the label fails to declare egg and wheat, which are common allergens present in the product.

    Product
    House Made Tarragon Chicken Salad Sandwich, brand DishD'Lish. The label declares House Roasted Chicken Breast, Herbs, Fresh Tarragon, Arugula, Mayonnaise, and Whole Grain Bread.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0932-2023·2023-05-31

    Ultra Tuna Salad Sandwich recall: undeclared egg and wheat allergens

    Ultra Tuna Salad Sandwich sold in Washington contains undeclared egg and wheat allergens. The label fails to declare these common allergens, posing a risk to allergic consumers.

    Product
    Ultra Tuna Salad Sandwich, brand DishD'Lish. The label declares Albacore Tuna with Fresh Herbs, Mayo, Capers, Cucumbers, and pickles on Organic Whole Grain Bread. Served with Sweet Pickle Chips.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0928-2023·2023-05-31

    Cole Slaw Recalled Due to Undeclared Egg and Soy Allergens

    Washington Crab & Seafood Company recalls 463 cases of 16-ounce Cole Slaw sold in North Carolina and South Carolina. The product contains undeclared egg and soy allergens not listed on the label.

    Product
    COLE SLAW Ingredients: cabbage, mayonaise sugar, vinegar, celery seed, salt WT 16 oz WASHINGTON CRAB Carolina seafood
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0955-2023·2023-05-31

    Safeway Oatmeal Raisin Cookies Recalled for Undeclared Peanut and Soy Allergens

    Safeway brand Oatmeal Raisin Cookies (18 count) are being recalled due to undeclared peanut and soy allergens. Consumers with allergies to these ingredients should not consume the product.

    Product
    Oatmeal Raisin Cookies 18 Count, Safeway brand, packaged in a clear plastic hinged container, Net wt. 14oz. UPC 0 227862 70500 7. Distributed by Safeway Inc. Pleasanton, CA 94588. The Oatmeal Raisin scale label does include allergen advisory statement: Made in a facility that…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0755-2023·2023-05-31

    Injectable Drug Recalled for Unverified Sterility After FDA Inspection

    Central Admixture Pharmacy Services is recalling 1673 bags of HyperLyte CR Injection due to lack of sterility assurance. An FDA inspection raised questions about whether the product met sterility standards.

    Product
    HyperLyte CR Injection, 250 mL bag, Rx only, Central Admixture Pharmacy Services, 6580 Snowdrift Road, Allentown, PA 18106, NDC 71285-8094-2, code 7128580942.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0702-2023·2023-05-31

    OxyTOCIN-dextrose injectable recalled nationwide for sterility assurance concerns

    Central Admixture Pharmacy Services is recalling oxyTOCIN 20 units in dextrose 5%/Lactated Ringer's solution nationwide due to lack of sterility assurance identified during FDA inspection. 7,595 bags across multiple lot numbers are affected.

    Product
    oxyTOCIN 20 units added to dextrose 5%/Lactated Ringer's 1,000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6031-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0698-2023·2023-05-31

    FDA Recalls Neonatal Parenteral Nutrition Bags for Sterility Concerns

    Central Admixture Pharmacy Services recalled 328 neonatal parenteral nutrition bags nationwide due to FDA concerns about product sterility after an inspection.

    Product
    Neonatal PN Starter Bag, Amino Acids (Trophamine) 3.5%/Dextrose 10% with low calcium and HEPARIN, packaged in 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100 Allentown, PA 18106, NDC 71285-0429-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0901-2023·2023-05-31

    Country Cookie Oatmeal Scotchie Cookies Recalled for Undeclared Milk Allergen

    Country Cookie LLC. is recalling Oatmeal Scotchie cookies because milk is present in the product but not declared on the allergen statement. Consumers with milk allergies should not consume these products.

    Product
    Country Cookie Oatmeal Scotchie cookie, plastic wrapped
    Category
    Food
    Distribution
    2 states