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.

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20226–20250 of 39655

  • SevereFDA (Food)·F-2395-2017·2017-07-05

    Hampton Farms Recalls Organic Almonds for Listeria Contamination Risk

    Severn Peanut Co. is recalling Avas Organic Roasted Unsalted Almonds due to potential Listeria monocytogenes contamination. The product was distributed in New Jersey, New York, Pennsylvania, and Connecticut.

    Product
    Avas 8 oz. Organic Roasted Unsalted Almonds UPC 8-10111-01032-0
    Category
    Food
    Distribution
    4 states
  • SevereUSDA FSIS·080-2017·2017-07-01

    Willow Tree Poultry Farm Recalls Chicken Salad Due To Undeclared Tuna

    Willow Tree Poultry Farm is recalling buffalo style chicken salad products because they contain undeclared tuna and are mislabeled.

    Product
    WILLOW TREE POULTRY FARM, INC. — Willow Tree Poultry Farm Recalls Chicken Salad Products Due To Misbranding And Undeclared Allergens
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·17V424000·2017-06-30

    Acura Recalls 2017 MDX Sport Hybrid for Fuel Hose Misrouting

    Honda is recalling 2017 Acura MDX Sport Hybrid vehicles because fuel hoses may be misrouted, potentially causing a fuel leak and fire risk.

    Product
    ACURA — ACURA MDX SPORT HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V413000·2017-06-29

    Newmar Recalls 2018 Motorhomes Due to Fuel Pump Drive Gear Slip Risk

    Newmar is recalling 2018 London Aire, King Aire, and Essex motorhomes because a fuel pump drive gear could slip, causing an engine stall and increasing crash risk.

    Product
    NEWMAR — NEWMAR KING AIRE, ESSEX, LONDON AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V412000·2017-06-29

    GM Recalls 2016-2017 Buick Envision for Headliner Safety Defect

    General Motors is recalling 2016-2017 Buick Envision vehicles because replacement headliners may lack required impact-absorbing foam, increasing injury risk in crashes.

    Product
    BUICK — BUICK ENVISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V415000·2017-06-29

    Lexus Recalls 2017 ES350 Vehicles Due to Steering Tie Rod Defect

    Toyota is recalling 2017 Lexus ES350 vehicles because the right-hand tie rod lock nut may loosen, potentially causing loss of steering and increasing crash risk.

    Product
    LEXUS — LEXUS ES350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V429000·2017-06-29

    Mazda Recalls Vehicles Due to Passenger Air Bag Inflator Rupture Risk

    Mazda is recalling 2007-2011 CX-7, CX-9, and 2009-2011 Mazda6 vehicles because the passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    MAZDA — MAZDA CX-7, CX-9, MAZDA6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V417000·2017-06-29

    Honda Recalls 2007-2011 CR-V Vehicles for Air Bag Inflator Defect

    Honda is recalling 2007-2011 CR-V vehicles where the passenger air bag inflator may have an incorrect wire harness, potentially preventing deployment in a crash.

    Product
    HONDA — HONDA CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·17182·2017-06-28

    South Shore Recalls 5-Drawer Chests Due to Tip-Over Hazard

    South Shore Industries is recalling about 68,300 Summer Breeze style 5-drawer chests because they are unstable and can tip over if not anchored to the wall. Consumers should stop using the chests until they are secured or contact the company for a refund or free restraint kit.

    Product
    5-drawer chests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2372-2017·2017-06-28

    Monfitello recalls Private Selection Peri Peri chili paste for peanut content

    Monfitello is recalling Private Selection African-Inspired Peri Peri Chili Culinary Spice Paste because the product may contain peanuts.

    Product
    PRIVATE SELECTION AFRICAN - INSPIRED PERI PERI CHILI CULINARY SPICE PASTE NET WT 4 OZ (113g) UPC 0 11110 80699 4 DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202 MADE IN CANADA
    Category
    Food
    Distribution
    31 states
  • SevereFDA (Devices)·Z-2224-2017·2017-06-28

    Vascular Solutions Recalls Venture Catheters Due to Material Detachment Risk

    Vascular Solutions, Inc. is voluntarily recalling Venture RX, OTW, and CS catheters because material may detach from the distal tip during use.

    Product
    Venture RX Catheter, Model 5820; Venture OTW Catheter, Model 5821; Venture CS Catheter, Model 5822. Sterilized using ethylene oxide, Rx Only. The Venture catheter is indicated for directing, steering, controlling, and supporting a guidewire to access discrete regions of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2373-2017·2017-06-28

    Monfitello Peruvian Inspired Aji Amarillo Culinary Spice Paste Recalled for Peanut Allergen

    Monfitello is recalling Private Selection Peruvian Inspired Aji Amarillo Culinary Spice Paste because it may contain peanuts. Consumers should stop using the product.

    Product
    Private Selection Peruvian Inspired Aji Amarillo Culinary Spice Paste NET WT 4 OZ (113g) INGREDIENTS: SOY SAUCE***CONTAINS: SOY. DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202 MADE IN CANADA
    Category
    Food
    Distribution
    31 states
  • SevereFDA (Devices)·Z-2616-2017·2017-06-28

    DePuy Mitek LATARJET Coracoid Drill Recalled for Breakage Risk

    DePuy Mitek is recalling LATARJET Coracoid Drills because the Combo Screw Driver tip may break during surgery.

    Product
    DePuy Mitek LATARJET EXPERIENCE Coracoid Drill Product Code: 288201 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Food)·F-2384-2017·2017-06-28

    Genetic Edge Compounds Recalls GEC TNT Thermanite Dietary Supplement

    Genetic Edge Compounds LLC is recalling GEC TNT Thermanite dietary supplements because the product contains DMAA and Methylsynephrine.

    Product
    GEC TNT Thermanite 60 Capsules Dietary Supplement in clear plastic bottle, UPC: 689466706222.
    Category
    Food
    Distribution
    21 states
  • SevereFDA (Food)·F-2381-2017·2017-06-28

    H & C Food Inc Recalls Lobster Flavored Balls for Undeclared Egg

    H & C Food Inc is recalling 300 cases of Lobster Flavored Balls distributed in New York because the product may contain undeclared egg.

    Product
    Master Carton is Labeled As: LOBSTER FLAVORED BALL DISTRIBUTED EXCLUSIVELY BY: H & C FOOD INC. BROOKLYN, NY 11237 KEEP FROZEN AT -18 C
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-2387-2017·2017-06-28

    Herbmed USA Recalls NutriHeal Cholesterol Supplement Due to Undeclared Milk

    Herbmed USA Company Inc. is recalling NutriHeal OPTIMAL CHOLESTEROL herbal supplements because they contain undeclared milk.

    Product
    NutriHeal OPTIMAL CHOLESTEROL Traditional Vegetarian Blend Herbal Supplement, 60 Tablets. Distributed By: Herbmed USA Company Inc.
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·17V410000·2017-06-28

    Lakota Colt Trailers Recalled Due to Furnace Venting Defect

    Lakota Corporation is recalling 2018 Colt trailers because the furnace flue may be improperly installed, preventing proper venting. This defect can cause carbon monoxide buildup inside the trailer, posing a risk of injury or death.

    Product
    LAKOTA — LAKOTA COLT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·079-2017·2017-06-28

    Vinh Hoan USA Recalls Frozen Swai Fillets Due to Import Violations

    Vinh Hoan USA is recalling approximately 84,000 pounds of frozen Swai fillets that entered U.S. commerce without meeting federal import requirements.

    Product
    Vinh Hoan USA, Inc. Recalls Siluriformes Fish Products Due To Failure To Comply With FSIS Import Requirements
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-2617-2017·2017-06-28

    DePuy Mitek LATARJET Drill Tip Recall Due to Breakage Risk

    DePuy Mitek is recalling LATARJET Coracoid Top Hat Drills because the Combo Screw Driver tip may break during surgery.

    Product
    DePuy Mitek LATARJET EXPERIENCE Coracoid Top Hat Drill Product Code: 288202 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0922-2017·2017-06-28

    Vi-Jon Recalls Magnesium Citrate Saline Laxative Due to Glass Particles

    Vi-Jon, Inc. is recalling 52,212 bottles of Magnesium Citrate Saline Laxative because glass particles were found in the product.

    Product
    Magnesium Citrate Saline Laxative Cherry Flavored, packaged in a) 10 fl. oz. (296 mL) bottle UPC: 072785104556 (Rexall's label), b) 10 fl. oz. (296 mL) bottle UPC: 041163254138 (Equaline's label), OTC, Distributed by a) Dolgencorp, LL, Goodlettsville, TN 37072 b)Supervalu, Inc.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2389-2017·2017-06-28

    Blue Diamond Blanched Diced Almonds Recalled for Salmonella Risk

    Blue Diamond Growers is recalling blanched diced almonds after a customer reported a positive Salmonella test result upon receipt.

    Product
    Blue Diamond Almonds Blanc DCD FN C (blanched diced fine); NET WT 11.34 Kg, 25 lbs. corrugated carton with poly liner; Product of the USA. Blue Diamond Almonds, Sacramento, CA
    Category
    Food
    Distribution
    5 states