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

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

18576–18600 of 39605

  • SevereFDA (Devices)·Z-1071-2018·2018-03-21

    Zimmer Biomet Recalls TunneLoc Tibial Fixation Devices Due to Sterilization Concerns

    Zimmer Biomet is recalling 14,461 TunneLoc Tibial Fixation Devices because gamma sterilization testing suggests the sterilization dose may be inadequate.

    Product
    TunneLoc Tibial Fixation Device Product Usage: To provide fixation of soft tissue grafts within the tibial tunnel during anterior cruciate ligament (ACL) and/or posterior cruciate ligament (PCL) reconstruction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·025-2018·2018-03-21

    California Jerky Factory Recalls Beef Jerky Due to Processing Deviation

    California Jerky Factory is recalling approximately 1,238 pounds of beef jerky products due to a processing deviation that may have led to under-processing.

    Product
    California Jerky Factory, Inc. — California Jerky Factory, Inc. Recalls Beef Jerky Products Due to Possible Processing Deviation
    Category
    Food
    Distribution
    3 states
  • SevereUSDA FSIS·024-2018·2018-03-20

    Mickey Brown Recalls Beef Burritos Produced Without Federal Inspection

    Mickey Brown, Inc. is recalling beef burrito products produced without federal inspection. No adverse reactions have been reported.

    Product
    Mickey Brown, Inc. — Mickey Brown, Inc Recalls Beef Burrito Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·18V179000·2018-03-19

    Forest River Recalls Motorhomes Due to Power Steering Hose Fire Risk

    Forest River is recalling specific 2012-2017 motorhomes because an incorrectly routed power steering hose may rub against the starter motor, causing electrical arcing and a fire risk.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN, GLAVAL BUS CHARLESTON, BERKSHIRE, PATHFINDER, CROSS COUNTRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V182000·2018-03-19

    McElrath Trailers Recalling 2013-2018 Models Due to Weld Failure Risk

    McElrath Trailers is recalling specific 2013-2018 models because a weld on the trailer neck may fail, potentially causing loss of control and a crash.

    Product
    MCELRATH TRAILERS — MCELRATH TRAILERS VX50-800, 818I, VX30-800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V181000·2018-03-19

    Entegra Aspire Recalled for Power Steering Hose Fire Risk

    Entegra Coach is recalling 2011-2012 and 2015-2016 Aspire motorhomes because an incorrectly routed power steering hose may cause electrical arcing and a fire.

    Product
    ENTEGRA — ENTEGRA ASPIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V183000·2018-03-19

    REV Recalls 2018 Motorhomes Due to HVAC Fire Risk

    REV Recreation Group is recalling 600 2018 motorhomes because HVAC wires may disconnect, creating a fire risk if reconnected incorrectly.

    Product
    MONACO — MONACO, AMERICAN COACH, FLEETWOOD SIGNATURE, MARQUIS, AMERICAN REVOLUTION, AMERICAN DREAM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·023-2018·2018-03-16

    Stampede Meat Recalls Beef Steaks Due to Salmonella Risk

    Stampede Meat is recalling approximately 484,800 pounds of frozen raw beef top sirloin steaks because a seasoning ingredient tested positive for Salmonella.

    Product
    Stampede Culinary Partners, Inc. — SMI Holdings, Inc Recalls Beef Products Due to Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18T002000·2018-03-16

    Les Schwab Recalls Retreaded Truck Tires Due to Adhesion Defect

    Les Schwab is recalling specific retreaded steel-belted radial truck tires because the vulcanizing compound may not have fully cured, increasing the risk of tread separation and crashes.

    Product
    TIRES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V178000·2018-03-15

    Hino Recalls 2018-2019 Trucks Due to Engine Valve Train Defect

    Hino is recalling 2018-2019 NE8J, NJ8J, and NV8J trucks because engine valve train lock nuts may be loose, potentially causing engine damage and shutdown.

    Product
    HINO — HINO NJ8J, NV8J, NE8J
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·022-2018·2018-03-15

    Standard Meat Company Recalls Raw Beef Steaks Due to Salmonella Risk

    Standard Meat Company is recalling raw beef top sirloin steaks that may be contaminated with Salmonella. The products were shipped to restaurants nationwide.

    Product
    Standard Meat Company — Standard Meat Company Recalls Beef Products Due to Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·021-2018·2018-03-15

    Johnsonville Recalls Smoked Pork Sausage Due to Possible Plastic Contamination

    Johnsonville is recalling approximately 109,603 pounds of smoked pork sausage products that may contain hard, green plastic pieces.

    Product
    Johnsonville, LLC — Johnsonville, LLC Recalls Smoked Pork Sausage Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0593-2018·2018-03-14

    Bella Capsules Recalled for Undeclared Sibutramine Content

    Bella All Natural is recalling Bella Capsules because they contain undeclared sibutramine, a withdrawn controlled substance, making them unapproved drugs.

    Product
    Bella Capsules, 600mg, 30-count bottles, Manufactured for: Bella All Natural 304 E 11th Street, Los Angeles, CA 90015
    Category
    Drug
    Distribution
    1 state
  • CriticalFDA (Food)·F-0910-2018·2018-03-14

    Lotte Kancho Choco-Biscuit Recalled for Undeclared Peanut Allergen

    Lotte International America Corp. is recalling Lotte Kancho Choco-Biscuit products because peanut allergen was found during product sampling and testing.

    Product
    Lotte Kancho Choco-Biscuit; Sold as Lotte Kancho - 42 g -1.48 oz. UPC CODE: 8801062 144815; Lotte Kancho Cup - 95 g cup - UPC CODE: 8801062 516858; Lotte Kancho Multi - 168 g - UPC CODE: 8801062 144815. Master carton UPC: 1 8801062 133090 Ingredients: Wheat Flour…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0909-2018·2018-03-14

    La Pasta Recalls Heinen's Potato Gnocchi for Undeclared Milk Allergen

    La Pasta, Inc. is recalling Heinen's Potato Gnocchi 9 oz. due to an undeclared milk allergen. The product was distributed in Illinois and Ohio.

    Product
    HEINEN'S Potato Gnocchi * Preservative Free * 9 oz. (225 g) in clear film plastic trays
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0579-2018·2018-03-14

    Apollo Care Recalls Vancomycin IV Bags Due to Stability Data Issues

    Apollo Care is recalling 360 bags of Vancomycin IV solution because stability data does not support the assigned 90-day beyond use date.

    Product
    Vancomycin 1g added to 250mL of 0.9% Sodium Chloride IV bag, Rx only, APOLLOcare, 3801 Mojave Ct., Suite 101, Columbia, MO 65202, NDC 71170-254-25.
    Category
    Drug
    Distribution
    1 state
  • SevereNHTSA·18V172000·2018-03-14

    KME Predator Fire Apparatus Recalled for Front Axle Spindle Defect

    Kovatch Mobile Equipment is recalling specific KME Predator fire apparatus vehicles because inconsistent machining may cause front axle spindles to crack and fail, potentially leading to wheel separation.

    Product
    KME — KME PREDATOR TANKER, PREDATOR RESCUE, PREDATOR AERIAL, PREDATOR PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V173000·2018-03-14

    Maserati Recalls 2017 Quattroporte and Ghibli for Engine Software Defect

    Maserati is recalling 2017 Quattroporte and Ghibli vehicles because an engine software issue may cause the transmission to shift into neutral or the engine to shut off unexpectedly.

    Product
    MASERATI — MASERATI QUATTROPORTE, GHIBLI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0908-2018·2018-03-14

    FDA Recalls 163 Endo GIA Radial Reloads Due to Manufacturing Error

    The FDA is recalling 163 Endo GIA Radial Reloads with Tri-Staple Technology because the device cartridge disengaged during use due to a manufacturing error.

    Product
    Endo GIA" Radial Reload with Tri-Staple" Technology The Endo GIA radial reloads with Tri-Staple Technology have application in open or minimally invasive general abdominal, gynecologic and thoracic surgery for resection and transection of tissue and creation of anastomosis…
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0580-2018·2018-03-14

    Apollo Care Recalls Vancomycin IV Bags Due to Unsupported Expiry Date

    Apollo Care is recalling 312 bags of Vancomycin IV solution because stability data does not support the assigned 90-day beyond use date.

    Product
    Vancomycin 1.25g added to 250mL of 0.9% Sodium Chloride IV bag, Rx only, APOLLOcare, 3801 Mojave Ct., Suite 101, Columbia, MO 65202, NDC 71170-264-25.
    Category
    Drug
    Distribution
    1 state