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.

Filters

Agency

Category

Minimum severity

Clear filters

10376–10400 of 36631

  • SevereNHTSA·20V730000·2020-11-24

    Ford Recalls 2020 Explorers Due to Fuel Tank Weld Defect

    Ford is recalling 2020 Explorers with 2.3L engines because an incomplete weld on the fuel tank inlet check valve could cause a fuel leak and fire during a crash.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V721000·2020-11-20

    Isuzu and Chevrolet Recall 2020 Trucks for Wiring Chafe Risk

    Isuzu and Chevrolet are recalling 2020 NPR-HD and 4500 Crew Cab trucks because a chafing wire harness or hose could cause a short circuit, engine stall, or fire.

    Product
    ISUZU — ISUZU, CHEVROLET NPR HD, LOW CAB FORWARD 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V720000·2020-11-20

    Isuzu and Chevrolet Trucks Recalled for Battery Cable Fire Risk

    Isuzu and Chevrolet are recalling 2020 NPR-HD and 4500 trucks because a battery cable may overheat near the exhaust, posing a fire risk.

    Product
    ISUZU — ISUZU, CHEVROLET NPR HD, LOW CAB FORWARD 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V722000·2020-11-20

    Triple E Recalls Motorhomes Due to Chafed Wire Harness and Tail Light Loss

    Triple E is recalling 2018-2021 Unity and Serenity motorhomes because a shifting water tank bracket can chafe the wire harness, causing tail lights to fail and increasing crash risk.

    Product
    TRIPLE E — TRIPLE E UNITY, SERENITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0102-2021·2020-11-18

    Meijer Fruit Tray With Dip Recalled for Potential Salmonella Risk

    Meijer is recalling Fresh From Meijer Fruit Tray with Dip due to a potential risk of Salmonella. The product was sold in six states.

    Product
    FRESH FROM MEIJER FRUIT TRAY WITH DIP, 49oz Clear plastic container, UPC 219248610449
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-0103-2021·2020-11-18

    Meijer Fruit Tray Recalled for Potential Salmonella Risk

    Meijer is recalling Fresh From Meijer Fruit Trays due to a potential risk of Salmonella. The product was sold in six states between September 26 and October 5.

    Product
    FRESH FROM MEIJER FRUIT TRAY, 49oz Clear plastic container, UPC 219214610008
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-0108-2021·2020-11-18

    Meijer Berry Explosion Cups Recalled for Potential Salmonella Risk

    Meijer is recalling 1,280 units of Fresh from Meijer Berry Explosion Cups due to a potential risk of Salmonella. The products were sold in six states.

    Product
    FRESH FROM MEIJER GS BERRY EXPLOSION CUP 6 OZ, 6oz Clear plastic container, UPC 219717302295
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-0127-2021·2020-11-18

    J&O Mixed Veggie Cup Recalled for Undeclared Egg Allergen

    Russ Davis Wholesale is recalling J&O Mixed Veggie Cups with Dip because they contain undeclared egg. The product was sold in five states.

    Product
    J&O Mixed Veggie Cup with Dip, Net Weight 5.0 oz. (128 g), UPC 95631-85818. Mfg By: RDW, Pueblo CO 81001
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0098-2021·2020-11-18

    Meijer Recalls Cantaloupe and Honeydew Slices Due to Salmonella Risk

    Meijer is recalling 24oz containers of Fresh from Meijer Cantaloupe and Honeydew Slices due to a potential risk of Salmonella. The product was sold in six states.

    Product
    FRESH FROM MEIJER CANTALOUPE AND HONEYDEW SLICES, 24oz Clear plastic container, UPC 220219600079
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-0107-2021·2020-11-18

    Meijer Strawberry and Pineapple Cup Recalled for Salmonella Risk

    Meijer is recalling 1,300 units of Fresh from Meijer Strawberry/Pineapple Cups due to a potential risk of Salmonella. The product was sold in six states.

    Product
    FRESH FROM MEIJER GS STRAWBERRY/PINEAPPLE CUP 6 OZ, 6oz Clear plastic container, UPC 219711302291
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-0115-2021·2020-11-18

    Starwest Botanicals Recalls Organic Elderberry Due to Salmonella Risk

    Starwest Botanicals is recalling organic elderberry because a customer test detected Salmonella. The product was distributed nationwide and to two Canadian customers.

    Product
    Elderberry Whole Organic; Sambucus Nigra; Origin: Croatia Distributed in boxes with plastic liners. Various sizes Bulk UPC 7 67963 07314 3, Item # 209290-00 Starwest Botanicals,Inc. 161 Main Street, Sacramento, CA 95838 Certified Organic
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0097-2021·2020-11-18

    Meijer Cantaloupe Chunks Recalled for Potential Salmonella Risk

    Meijer is recalling Fresh from Meijer Cantaloupe Chunks due to a potential risk of Salmonella. The products were sold in six states.

    Product
    FRESH FROM MEIJER CANTALOUPE CHUNKS LARGE BOWL, 32oz Clear plastic container, UPC 219323109721. FRESH FROM MEIJER CANTALOUPE CHUNKS SMALL BOWL, 16oz Clear plastic container, UPC 220196109725. FRESH FROM MEIJER CANTALOUPE CHUNKS KOSHER - LG, 32oz Clear plastic container, UPC 220
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-0096-2021·2020-11-18

    IncredibleStoneCrab Mustard Sauce Recalled for Undeclared Allergens

    Incredible Fish is recalling 181 containers of IncredibleStoneCrab Mustard Sauce due to undeclared fish, egg, and milk allergens.

    Product
    IncredibleStoneCrab, Mustard Sauce, 8 oz. plastic container, Distributed by: IncredibleStoneCrab,
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·20V713000·2020-11-18

    Lamborghini Recalls 2019-2020 Urus Vehicles Due to Fuel Line Fire Risk

    Lamborghini is recalling 2,831 2019-2020 Urus vehicles because high engine temperatures may damage the fuel line connector, causing a leak and increasing fire risk.

    Product
    LAMBORGHINI — LAMBORGHINI URUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0072-2021·2020-11-18

    H & H Remedies Recalls White Liniment Due to CGMP Deviations

    H & H Remedies, LLC is voluntarily recalling 365 bottles of White Liniment due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    White Liniment packaged in a) 1 oz; b) 4 oz.; and c) 6 oz bottles. Mfg & Sold by: H & H Remedies, LLC c/o David A. Cox, 1219 South Broadway, New Philadelphia, OH 44663
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0430-2021·2020-11-18

    Stereotaxis Niobe ES System Recalled for Potential Fire Hazard

    Stereotaxis Inc is recalling 121 Niobe ES Systems due to a potential fire risk in the internal computer cabinet.

    Product
    Niobe ES System, Models 001-006000-1 and 001-006100-1
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·20V714000·2020-11-18

    Alfa Romeo Giulia Recall for Rear Brake Disc Fracture Risk

    FCA US LLC is recalling 2020 Alfa Romeo Giulia vehicles because rear brake discs may fracture, potentially reducing braking performance and increasing crash risk.

    Product
    ALFA ROMEO — ALFA ROMEO GIULIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0099-2021·2020-11-18

    Meijer Triple Treat & Melon Recalled for Potential Salmonella Risk

    Meijer is recalling Fresh from Meijer Triple Treat & Melon due to a potential risk of Salmonella. The product was sold in six states.

    Product
    FRESH FROM MEIJER TRIPLE TREAT & MELON, 22oz Clear plastic container, UPC 220453514736
    Category
    Food
    Distribution
    6 states
  • SevereNHTSA·20V715000·2020-11-18

    Keystone Outback trailers recalled for potential frame rail buckling defect

    Keystone is recalling 2019–2021 Outback recreational trailers for inadequate frame rail support that may cause buckling and crash risk. Owners should contact 1-866-425-4369 for the free frame reinforcement repair.

    Product
    KEYSTONE — KEYSTONE OUTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0431-2021·2020-11-18

    Stryker Recalls Cranial Perforators Due to Potential Metal Fragment Risk

    Stryker is recalling Zyphr Disposable Cranial Perforators because a crack in the inner bit could release metal fragments into the surgical site or cause delayed disengagement.

    Product
    Stryker Zyphr Disposable Cranial Perforator, Large 14/11 mm- is a sterile, single use cutting accessory intended for cutting an 11 mm diameter access hole through the cranium of adult patients. Catalog Number: 5100-060-001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0076-2021·2020-11-18

    Baxter Recalls Bupivacaine Injection Due to Particulate Matter

    Baxter Healthcare is recalling specific lots of Bupivacaine Hydrochloride Injection due to the presence of black and transparent particles in the solution.

    Product
    Bupivacaine Hydrochloride in 8.25% Dextrose Injection, USP Spinal 0.75% (15 mg/2 mL) 10 x 2 mL single-dose ampules, Rx only, Manufactured for: Baxter Healthcare Corporation Deerfield, IL 60015 USA, Manufactured by: Baxter Pharmaceuticals India Private Ltd Ahmedabad 382213 India,
    Category
    Drug
    Distribution
    Distributed nationwide