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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29951–29975 of 39756

  • SevereFDA (Devices)·Z-0206-2015·2014-12-03

    Philips Medical Systems Recalls Gel-E and Squishon Baby Support Products Due to Mold

    Philips Medical Systems is recalling Gel-E Donut and Squishon 2 baby support products because mold was found on the gel-filled items.

    Product
    Gel-E Donut : 92025-A (Extra Small), 92025-B (Small), 92025-C (Medium) and Squishon 2 91033-2. The products are intended to support and cradle a baby's head and/or body.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0564-2015·2014-12-03

    MaraNatha Peanut Butter Recalled for Potential Salmonella Contamination

    nSpired Natural Foods is recalling MaraNatha No Stir Creamy Peanut Butter due to potential Salmonella contamination. The product was distributed in the US, Canada, and other countries.

    Product
    MaraNatha No Stir Creamy Peanut Butter, 16 oz., UPC 51651092210; MaraNatha No Stir Creamy Peanut Butter, 500 gram, UPC 51651093408.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0589-2015·2014-12-03

    Marathon Ventures Recalls Macadamia Nuts Due to Salmonella Florida Contamination

    Marathon Ventures Inc. is recalling various brands of macadamia nuts nationwide due to possible contamination with Salmonella florida.

    Product
    Macadamia nuts in various formats: (1.) Western Family Macadamia Diced Nuts, Net Wt 5 oz. plastic bags Distributed by:Western Family Foods, Inc. Portland, OR UPC 0 15400 16635 5 (2.) Shur Fine Macadamia Diced Nuts, Net Wt 5 oz. plastic bags. Distributed by:Western Family…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0260-2015·2014-12-03

    Perry Drug Recalls Methyl B12 Syringes Due to Sterility Concerns

    Perry Drug Inc. is recalling 186 prefilled syringes of Methyl B12 injection due to potential sterility assurance issues identified during an FDA inspection.

    Product
    Methyl B12 25 mg/mL Inj., 10 Syringes, Compounded Rx, Perry Drug Compounding Pharmacy, Overland Park, KS --- NDC 88888-2014-37
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0272-2015·2014-12-03

    Perry Drug Recalls HCG Vials Due to Sterility Assurance Concerns

    Perry Drug Inc. is recalling HCG-20,000 U/2 mL vials in Kansas and Missouri due to quality control issues affecting sterility assurance.

    Product
    HCG-20,000 U/2 mL Vial, Compounded Rx, Perry Drug Compounding Pharmacy, Overland Park, KS ---NDC 88888-2195-47
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0262-2015·2014-12-03

    Perry Drug Recalls Leuprolide Micro Lupron Kits Due to Sterility Concerns

    Perry Drug Inc. is recalling Leuprolide 50 mcg/0.1 mL Micro Lupron Kits in Kansas and Missouri due to potential sterility assurance risks identified during an FDA inspection.

    Product
    Leuprolide 50 mcg/0.1 mL Micro Lupron Kit, 5Ml, Compounded Rx, Perry Drug Compounding Pharmacy, Overland Park, KS --- NDC 88888-1124-57
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Food)·F-0551-2015·2014-12-03

    Almond Butter Recalled for Potential Salmonella Contamination

    nSpired Natural Foods is recalling specific almond butter products due to potential Salmonella contamination. Consumers should stop using and return the products.

    Product
    MaraNatha Organic Roasted Creamy Almond Butter, 16 oz., UPC 51651060219; Whole Foods 365 Organic Creamy Almond Butter, 16 oz., UPC 99482405960.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0264-2015·2014-12-03

    Perry Drug Recalls Testosterone Cyp Syringes Due to Sterility Concerns

    Perry Drug Inc. is recalling Testosterone Cyp 200 mg/mL syringes due to quality control issues affecting sterility assurance.

    Product
    Testosterone Cyp 200 mg/mL Sesame Inj., 4Ml Syringes, Compounded Rx, Perry Drug Compounding Pharmacy, Overland Park, KS --- NDC 88888-7906-71
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0226-2015·2014-12-03

    Synthes Recalls Titanium Polyaxial Reduction Heads for Spine Screws

    Synthes (USA) Products LLC is recalling 24 Titanium Polyaxial Reduction Heads for Matrix Spine Screws because the inner diameter may not have been machined to the correct specification.

    Product
    Synthes Titanium Polyaxial Reduction Head for Titanium Matrix Spine Screws: The Titanium Polyaxial Reduction Head is a part of the Matrix Spine System. Intended for posterior pedicle screw fixation (Tl OS2- ilium), posterior hook fixation (Tl-L5), or anterolateral fixation…
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0280-2015·2014-12-03

    Hospira Recalls IV Bags Due to Potential Sterility Breach

    Hospira is recalling 823,296 bags of 5% Dextrose and 0.45% Sodium Chloride Injection due to potential punctures that may compromise sterility.

    Product
    5% Dextrose and 0.45% Sodium Chloride Injection, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7926-09.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0274-2015·2014-12-03

    Perry Drug Recalls Compounded HCG Injections Due to Sterility Concerns

    Perry Drug Inc. is recalling compounded HCG injections in Kansas and Missouri due to potential sterility assurance issues identified during an FDA inspection.

    Product
    HCG - 10,000 Unit PF Inject, 1mL Syringe, Compounded Rx, Perry Drug Compounding Pharmacy, Overland Park, KS NDC 88888-0216-49
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0265-2015·2014-12-03

    Perry Drug Recalls HCG Vials Due to Sterility Assurance Concerns

    Perry Drug Inc. is recalling HCG Low Dose vials in Kansas and Missouri due to quality control issues affecting sterility assurance.

    Product
    HCG Low Dose 30 IU/0.1 mL, 5 Ml vial, Compounded Rx, Perry Drug Compounding Pharmacy, Overland Park, KS --- NDC 88888-0231-54
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0277-2015·2014-12-03

    Hospira Recalls Normosol-R IV Bags Due to Sterility Concerns

    Hospira is recalling 152,172 bags of Normosol-R IV solution due to potential punctures that may compromise sterility and cause leaks.

    Product
    Normosol-R pH 7.4 Multiple Electrolytes Injection Type 1, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7670-09.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V763000·2014-12-01

    Subaru Recalls 2003-2005 Models for Air Bag Inflator Rupture Risk

    Subaru is recalling 2003-2005 Legacy, Outback, and Baja vehicles in high-humidity areas because the passenger air bag inflator may rupture during deployment.

    Product
    SUBARU — SUBARU LEGACY, BAJA, OUTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V683000·2014-11-28

    Nissan and Infiniti Recall Vehicles for Fuel Pressure Sensor Defect

    Nissan is recalling specific 2012-2015 Nissan Juke and Infiniti models because loose fuel pressure sensors may cause fuel leaks and potential fires.

    Product
    INFINITI — INFINITI, NISSAN QX56, JUKE, M56, QX80
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V759000·2014-11-28

    Thomas Built Buses Minotour Recalled for Loose Fuel Tank Strap

    Daimler Trucks North America is recalling 2013-2015 Thomas Built Buses Minotour non-school buses because a loose fuel tank strap may allow the tank to contact the ground, increasing the risk of a fuel leak and fire.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V760000·2014-11-28

    Thomas Built Buses Recalls Minotour School Buses for Fuel Tank Strap Issue

    Daimler Trucks North America is recalling 2013-2015 Thomas Built Buses Minotour school buses because a loose fuel tank strap fastener could cause a fuel leak and fire.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V758000·2014-11-28

    Daimler Trucks Recalls 2015 Models Due to Brake Drag Risk

    Daimler Trucks North America is recalling 1,580 model year 2015 trucks because an improperly seated brake chamber diaphragm may cause brake drag, increasing the risk of a crash.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 4700, COLUMBIA GLIDER, 108SD, CORONADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0509-2015·2014-11-26

    Unity Groves Avocados Recalled Due to Salmonella Contamination

    Unity Groves Corporation is recalling avocados because FDA samples tested positive for Salmonella. The product was distributed in Florida and Texas.

    Product
    Avocado label: Unity Groves Avocados # 4221 Born in the USA Box label: Pride of the Redlands brand 32ct Green skin avocados, packaged in 1/2 BU Box
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Drugs)·D-0252-2015·2014-11-26

    Abrams Royal Pharmacy Recalls Trace Mineral-5 MDV Due to Non-Sterility

    Abrams Royal Pharmacy is recalling Trace Mineral-5 MDV vials because a contract laboratory identified Staphylococcus warneri in the product, indicating non-sterility.

    Product
    Trace Mineral-5 MDV, supplied in 10 mL vials, Each ML contains: 1 mg Zinc (as sulfate), 0.4 mg Copper (as sulfate), 0.1 mg Manganese (as sulfate), 4 mcg Chromium (as chloride), 20 mcg Selenium (as sodium), 0.9% Benzyl alcohol in water for injection, Rx Only, Compounded…
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0251-2015·2014-11-26

    Abrams Royal Pharmacy Recalls Non-Sterile Lidocaine and Bupivacaine Syringes

    Abrams Royal Pharmacy is recalling 50 syringes of a compounded lidocaine and bupivacaine mixture due to non-sterility. The products were distributed in Texas.

    Product
    Lidocaine 18.18 mg/mL/Bupivacaine 2.27 mg/mL/Epinephrine 0.0022 mg/mL/Hyaluronidase13.64 u/mL, supplied in 11 mL Sterile Syringes, Rx only, Compounded med, Single use only, (Red Block) ABRAMS ROYAL Compounding Pharmacy, Dallas, TX
    Category
    Drug
    Distribution
    1 state
  • CriticalFDA (Food)·F-0519-2015·2014-11-26

    Welcome Market Coconut Toast Recalled for Missing Allergen Statements

    Welcome Market Inc is recalling Coconut Toast products due to missing allergen statements for wheat, soy, and/or milk. The recall affects 3,133 loaves sold in Northern California and Washington.

    Product
    Coconut Toast, Net Wt 20 oz.. (1.25 lb) 99 Ranch Market 338 Barber Ln, Milpitas, CA 95035
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-0513-2015·2014-11-26

    New Hope Mills Recalls Gluten Free Chia Pancake Mix for Undeclared Soy

    New Hope Mills is recalling its Gluten Free Chia Pancake and Waffle Mix because it contains undeclared soy.

    Product
    NEW HOPE MILLS GLUTEN FREE CHIA PANCAKE & WAFFLE MIX, NET WT 16 OZ (1 LB) 454g, UPC 074703530126. Packed as 8 units per carton. Each unit is held within a red and white front box. Made in the USA.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0511-2015·2014-11-26

    M & M Farm Recalls Florida Avocados Due to Salmonella

    M & M Farm Inc. is recalling 30,000 lbs of M & M brand Number 2 Florida Avocados because FDA samples tested positive for Salmonella.

    Product
    M & M brand Number 2 Florida Avocados, packed in 50 lb cardboard boxes
    Category
    Food
    Distribution
    1 state