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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35276–35300 of 39756

  • SevereFDA (Devices)·Z-0872-2013·2013-02-27

    Hill-Rom Recalls Liko Overhead Rail Systems Due to Corrosion

    Hill-Rom is recalling Liko Overhead Rail Systems because hardware corrosion in high-humidity areas caused two rail failures.

    Product
    Liko Overhead Rail System, Ceiling Mounted Rail Systems for all Liko Stationary Lifts including Likorall, Multirall and Masterlift Systems Product Usage - The Overhead Rail System allows overhead lifts to be mounted to the ceiling allowing versatility for use in lifting…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1002-2013·2013-02-27

    Sara Lee Deluxe Bagels Recalled Due to Metal Fragments

    Bimbo Bakeries USA is recalling Sara Lee Deluxe Bagels in four varieties because metal fragments were found in two packages.

    Product
    Sara Lee Deluxe Bagels, 20 oz packages; BLUEBERRY, PLAIN, CINNAMON RAISIN,and HONEY WHEAT varieties.
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0828-2013·2013-02-27

    DePuy LPS Diaphyseal Sleeves Recalled for Potential Taper Fracture

    DePuy Orthopaedics is voluntarily recalling LPS Diaphyseal Sleeves because the taper connection may fracture under normal gait loads.

    Product
    LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are used with the LPS System which is an end-stage revision knee product that allows surgeons to reconstruct severe soft tissue and bony defects.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0844-2013·2013-02-27

    Codman NeuroPath Guiding Catheters Recalled for Potential Sterility Compromise

    Codman & Shurtleff is recalling 56 NeuroPath 6Fx90 Guiding Catheters because package integrity issues may compromise device sterility.

    Product
    NEUROPATH 6Fx90 GUIDING CATH HH Product Code: GHH60900000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0999-2013·2013-02-27

    Tumalo Farms Recalls Improperly Pasteurized Jewell Soft Brie-Style Cheese

    Tumalo Farms LLC is recalling 222 six-ounce pucks of Jewell soft brie-style cheese because it was improperly pasteurized. The product was distributed in Washington and Oregon.

    Product
    A soft brie-style cheese called Jewell. Ingredients: Certified organic cows' milk, Pasteurized farmstead goats' milk, cultures, rennet and salt. (information obtained from firm's web site)
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0862-2013·2013-02-27

    Codman & Shurtleff Recalls Neuropath Guiding Catheters Due to Sterility Concerns

    Codman & Shurtleff is recalling Neuropath 6Fx90 Guiding Catheters because package integrity issues may compromise device sterility. The recall covers 10 units distributed worldwide.

    Product
    NEUROPATH 6Fx90 GUIDING CATH MCV Product Code: GCB60900000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0829-2013·2013-02-27

    DePuy LPS Diaphyseal Sleeves Recalled for Potential Taper Fracture

    DePuy Orthopaedics is voluntarily recalling LPS Diaphyseal Sleeves because the taper connection may fracture under normal physiologic loads.

    Product
    LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are used with the LPS System which is an end-stage revision knee product that allows surgeons to reconstruct severe soft tissue and bony defects.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0849-2013·2013-02-27

    Codman & Shurtleff Recalls NeuroPath Guiding Catheters Due to Sterility Concerns

    Codman & Shurtleff is recalling 266 units of NeuroPath 6Fx100 Guiding Catheters because package integrity issues may compromise device sterility.

    Product
    NEUROPATH 6Fx100 GUIDING CATH ST Product Code: GST61000000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0857-2013·2013-02-27

    Codman NeuroPath Guiding Catheters Recalled for Potential Sterility Compromise

    Codman & Shurtleff is recalling NeuroPath 5Fx90 Guiding Catheters because package integrity issues may compromise device sterility.

    Product
    NEUROPATH 5Fx90 GUIDING CATH MPD Product Code: GMD50900000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V056000·2013-02-22

    Daimler Orion VII Transit Buses Recalled for Brake Chamber Leak

    Daimler Buses North America is recalling 2011-2012 Orion VII buses because leaking brake chambers may cause the parking brake to drag, potentially leading to overheated components and fire.

    Product
    ORION — ORION VII
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V058000·2013-02-22

    Porsche Recalls 2012-2013 911 Models for Exhaust Tail Pipe Fracture Risk

    Porsche is recalling 2012-2013 911 Carrera and Carrera 4 vehicles because the exhaust tail pipe may fracture and separate, posing a hazard to other vehicles.

    Product
    PORSCHE — PORSCHE 911 CARRERA 4, 911 CARRERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V076000·2013-02-22

    Fontaine Heavy-Haul Recalls 2013 Renegade Trailers Due to Structural Defect

    Fontaine Heavy-Haul is recalling 78 model year 2013 Renegade LX40 and LXT40 lowbed trailers because a connecting plate may crack and fail, increasing crash risk.

    Product
    FONTAINE — FONTAINE RENEGADE LXT40, RENEGADE LX40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0997-2013·2013-02-20

    Hoop Nuts Recalls Pistachios Due to Salmonella Contamination

    Hoop Nuts LLC is recalling dry roasted pistachios due to Salmonella contamination. The recall affects 20 cases distributed in California.

    Product
    ARO PISTACHIO/ ORANDI FARMS PISTACHIO HALVES N PIECES 30LB WHITE CORRUGATED BOXES-Pistachios Dry Roasted
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0992-2013·2013-02-20

    H-E-B Recalls General Joe's Chicken Deli Products Due to Salmonella Risk

    H-E-B is recalling General Joe's chicken deli products in Texas because they may be contaminated with salmonella. Consumers should not eat the recalled items.

    Product
    HEB Deli General Joes Chicken Entree, UPC 0026966900000; HEB Deli HE Bowl General Joes Chicken, UPC 0026967400000; HEB Deli General Joe's Chicken Retail Pack, UPC 0026520900000; HEB Deli General Joes Chicken UPC 0026703700000
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0996-2013·2013-02-20

    Hoop Nuts Recalls Pistachios Due to Salmonella Contamination

    Hoop Nuts LLC is recalling raw pistachios due to Salmonella contamination. The recall affects 20 cases of 30-pound boxes distributed in California.

    Product
    ARO PISTACHIO/ ORANDI FARMS PISTACHIO HALVES N PIECES 30LB WHITE CORRUGATED BOXES-Pistachios Raw
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0995-2013·2013-02-20

    HEB Deli Sweet and Sour Chicken Recalled for Salmonella Risk

    He Butt Grocery Company is recalling HEB Deli Sweet and Sour Chicken products in Texas due to potential Salmonella contamination.

    Product
    HEB Deli Sweet and Sour Chicken Entree UPC 0026967200000; HEB Deli HE Bowl Sweet and Sour Chicken UPC 0026967800000; HEB Deli Sweet and Sour Chicken UPC 0026705000000
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0749-2013·2013-02-20

    GE Healthcare Recalls Infant Resuscitation Systems Due to Reversed Fittings

    GE Healthcare is recalling 276 Giraffe and Panda Bag and Mask Resuscitation Systems because oxygen and air inlet fittings were reversed during assembly.

    Product
    Giraffe and Panda Bag and Mask Resuscitation System The T-piece Resuscitation System [ventilator, emergency powered resuscitator]/Panda Bag and Mask Resuscitation System provides the basic equipment required for pulmonary resuscitation of infants.
    Category
    Medical Device
    Distribution
    31 states
  • SevereFDA (Food)·F-0994-2013·2013-02-20

    HEB Deli Sesame Chicken Products Recalled for Salmonella Risk

    H-E-B is recalling four varieties of deli sesame chicken products sold in Texas due to potential salmonella contamination.

    Product
    HEB Deli Sesame Chicken Entree UPC 0026960600000; HEB Deli HE Bowl Sesame Chicken UPC 0026967700000; HEB Deli Sesame Chicken Retail Pack UPC 0026521900000; HEB Deli Sesame Chicken UPC 0026704500000
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0763-2013·2013-02-20

    St. Jude Medical Recalls TorqVue FX Delivery Systems Due to Fracture Risk

    St. Jude Medical is recalling 635 TorqVue FX Delivery Systems because the core wire could fracture during use.

    Product
    St. Jude Medical, AGA Medical corporation, AMPLATZER¿ TorqVue¿ FX Delivery System. Model #'s: 9-ITVFX06F45/60, 9-ITVFX07F45/60, 9-ITVFX007F45/80, 9-ITVFX08F45/60, 9-ITVFX08F45/80, 9-ITVFX09F45/80, 9-ITVFX10F45/80 9-ITVFX12F45/80, 9-ITVFX13F45/80. Cardiac surgical instrument…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0984-2013·2013-02-20

    Altiza Recalls Malichita Brand Cucumbers Due to Salmonella Contamination Risk

    Altiza Inc. is recalling Malichita brand cucumbers because they may be contaminated with Salmonella. The affected product was distributed in California.

    Product
    Cucumbers, 44 lbs/box. Brand: Malichita (green, yellow, red and white background color on each cartons)
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0993-2013·2013-02-20

    H-E-B Recalls Lemon Grass Chicken Deli Products Due to Salmonella Risk

    H-E-B is recalling specific Lemon Grass Chicken deli products in Texas due to potential Salmonella contamination.

    Product
    HEB Deli Lemon Grass Chicken Entree UPC 0026967100000; HEB Deli HE Bowl Lemon Grass Chicken UPC 0026967600000; HEB Deli Lemon Grass Chicken Retail Pack UPC 0026521800000; HEB Deli Lemon Grass Chicken UPC 0026705200000
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0974-2013·2013-02-20

    Suadel Empanadillas Recalled for Undeclared Wheat and Soy Allergens

    Suadel Food Products is recalling Empanadillas Sabor a Carne because wheat and soy are not declared on the label.

    Product
    "Estrella Food Products, Inc***Empanadillas Sabor a Carne(Meat flavorTurnovers)***5 units, 12 units and 24 units***Elaborado y Empacado por: Estrella Food Products, Inc., Bayamon, PR 00959-1906***".
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0795-2013·2013-02-20

    Lumenis Recalls VersaCut Tissue Morcellator for Labeling Corrections

    Lumenis Limited is recalling VersaCut Tissue Morcellator devices to correct labeling following three reported air embolism events caused by incorrect tubing hook-up.

    Product
    The Lumenis VersaCut Tissue Morcellator Product Usage: is intended for use under direct or endoscopic visualization for the morcellation and removal of dissected tissue during pelviscopic, laparoscopic, percutaneous, and open surgical procedures whenever access to the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0986-2013·2013-02-20

    Pamela's Chocolate Chunk Cookie Mix Recalled for Potential Glass or Plastic Fragments

    Pamela's Products is recalling 1,709 cases of Chocolate Chunk Cookie Mix due to potential glass or plastic fragments.

    Product
    Pamela's Chocolate Chunk Cookie Mix; Gluten Free, Wheat Free, Non Dairy 13.9 oz. package. UPC 93709-30050 Pamela's Products, Ukiah, CA 95482
    Category
    Food
    Distribution
    Distributed nationwide