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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16976–17000 of 39599

  • SevereFDA (Food)·F-0219-2019·2018-10-31

    McCain Recalls Fire Roasted Diced Yellow Peppers Due to Listeria and Salmonella

    McCain Foods USA is recalling Fire Roasted 1/2" Diced Yellow Peppers because products were released after presumptive positive tests for Listeria monocytogenes and Salmonella without confirmation.

    Product
    Fire Roasted 1/2" Diced Yellow Peppers: Sold in 25 lb. Brand Name: Jon-Lin¿
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0186-2019·2018-10-31

    Alcon Recalls CyPass Micro-Stent Implant Due to Endothelial Cell Loss

    Alcon is recalling the CyPass Micro-Stent implant because long-term study data showed statistically significant endothelial cell loss in patients.

    Product
    CyPass System 241, Intraocular Pressure Lowering Implant, CYPASS MICRO-STENT, CYPASS APPLIER, REF: 8065754001. For ophthalmic use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0095-2019·2018-10-31

    Pfizer Recalls Meropenem Injection Due to Loss of Sterility Assurance

    Pfizer is recalling 71,075 vials of Meropenem for Injection because the containers may have lost integrity, compromising sterility.

    Product
    Meropenem for Injection, USA (I.V.), 1 gram/vial, 25 vials per carton, Sterile, Rx Only, Manufactured for: Hospira, Inc., Lake Forest, IL 60045, USA. NDC carton: 0409-3506-01; NDC vial: 0409-3506-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0053-2019·2018-10-31

    Sprout Creek Farm Recalls Margie Cheese Due to Improper Pasteurization

    Sprout Creek Farm is recalling Margie Cheese because it was not properly pasteurized. The product was distributed in New York.

    Product
    Margie Cheese, Pasteurized Cow's Milk Cheese, Sprout Creek Farm Poughkeepsie, NY 12603 Plant # 36-8436
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0185-2019·2018-10-31

    Alcon Recalls CyPass Micro-Stent Due to Endothelial Cell Loss

    Alcon Research is recalling CyPass Micro-Stent devices because long-term study data showed statistically significant endothelial cell loss in patients.

    Product
    CyPass System 241-S, CYPASS MICRO-STENT, CYPASS LOADED, CYPASS APPLIER, REF CATALOG #: 8065754003 For ophthalmic use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V762000·2018-10-30

    Altec Recalls 2009 Aerial Devices Due to Riser Assembly Cracking Risk

    Altec Industries is recalling 2009 LSS 60 and LSS 70 Elevator Aerial devices because the elevator riser assembly may crack and fail, increasing the risk of injury or death.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V759000·2018-10-29

    2018 Jeep Grand Cherokee SRT and Trackhawk Floor Mat Recall

    Chrysler is recalling 2018 Jeep Grand Cherokee SRT and Trackhawk vehicles because the driver's floor mat may prevent the accelerator pedal from returning to idle, increasing crash risk.

    Product
    JEEP — JEEP GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·106-2018·2018-10-27

    Red Square Foods Recalls Frozen Meat and Poultry Products for Undeclared Allergens

    Red Square Foods is recalling frozen meat and poultry ravioli and blintzes because they contain undeclared eggs, milk, and wheat.

    Product
    Red Square Foods, Inc., Recalls Frozen Not-Ready-To-Eat Meat and Poultry Products due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·18V757000·2018-10-26

    Altec Recalls 2018 Digger Derricks and Aerial Devices for Fastener Failure

    Altec is recalling 2018 Digger Derricks and Aerial Devices because high-strength fasteners may fail, causing the pedestal to separate from the turn table and increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE, DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V755000·2018-10-25

    BMW Recalls Diesel Vehicles Due to EGR Cooler Leak Fire Risk

    BMW is recalling specific 2013-2018 diesel models because a leaking EGR cooler can cause the intake manifold to melt, increasing the risk of a fire.

    Product
    BMW — BMW 328D, X5, 535D, X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V754000·2018-10-25

    Kia Recalls 2018 Stinger Vehicles Due to Wiring Fire Risk

    Kia is recalling 2018 Stinger vehicles because a front wiring harness may be damaged by a burr, increasing the risk of a fire.

    Product
    KIA — KIA STINGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19015·2018-10-25

    Haier Top-Mount Refrigerators Recalled Due to Fire Hazard

    Haier America is recalling about 137,000 top-mount refrigerators because an electrical component can short circuit, posing a fire hazard.

    Product
    Haier Top-Mount Refrigerators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0420-2019·2018-10-24

    La Mexicana Peach Mango Salsa Recalled for Listeria Risk

    La Mexicana LLC is recalling Peach Mango Salsa in 16, 24, and 64 oz. sizes due to potential Listeria monocytogenes contamination.

    Product
    La Mexicana Peach Mango Salsa 16 oz., 24 oz., and 64 oz.
    Category
    Food
    Distribution
    22 states
  • CriticalFDA (Food)·F-0419-2019·2018-10-24

    La Mexicana Medium Salsa Recalled for Potential Listeria Contamination

    La Mexicana LLC is recalling various sizes of Medium Salsa due to potential Listeria monocytogenes contamination. The product was distributed in 22 U.S. states.

    Product
    La Mexicana Medium Salsa 16 oz., 24 oz., 48 oz., 64 oz., and 128 oz. Gourmet Style Medium Salsa 16 oz.
    Category
    Food
    Distribution
    22 states
  • CriticalFDA (Drugs)·D-0074-2019·2018-10-24

    CVS Sinus Relief Nasal Spray Recalled for Pseudomonas Contamination

    Product Quest Manufacturing LLC is recalling CVS-branded Sinus Relief nasal spray due to failed microbiological testing for Pseudomonas aeruginosa.

    Product
    Sinus Relief (oxymetazoline HCl) Nasal decongestant, 0.05%, 0.5 FL OZ (15 mL) bottle, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 43236 5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0417-2019·2018-10-24

    La Mexicana Hot Salsa Recalled for Potential Listeria Contamination

    La Mexicana LLC is recalling various sizes of Hot Salsa due to potential Listeria monocytogenes contamination. The product was distributed in 22 U.S. states.

    Product
    La Mexicana Hot Salsa 16 oz., 24 oz., 48 oz., 64 oz., and 128 oz. Gourmet Style Hot Salsa 16 oz.
    Category
    Food
    Distribution
    22 states
  • CriticalFDA (Food)·F-0418-2019·2018-10-24

    La Mexicana Mild Salsa Recalled for Potential Listeria Contamination

    La Mexicana LLC is recalling various sizes of Mild Salsa due to potential Listeria monocytogenes contamination. The product was distributed across 22 U.S. states.

    Product
    La Mexicana Mild Salsa 16 oz., 24 oz., 48 oz., 64 oz., and 128 oz. Gourmet Style Mild Salsa 16 oz. and 24 oz.
    Category
    Food
    Distribution
    22 states
  • CriticalFDA (Food)·F-0422-2019·2018-10-24

    La Mexicana Cantina Salsa Recalled for Potential Listeria Contamination

    La Mexicana LLC is recalling specific sizes of Cantina Salsa due to potential Listeria monocytogenes contamination. The product was distributed in 22 U.S. states.

    Product
    La Mexicana Cantina Salsa 14 oz., 24 oz., and 64 oz.
    Category
    Food
    Distribution
    22 states
  • CriticalFDA (Food)·F-0421-2019·2018-10-24

    La Mexicana Garlic Salsa Recalled for Potential Listeria Contamination

    La Mexicana LLC is recalling 780,000 units of Garlic Salsa due to potential Listeria monocytogenes contamination. The product was distributed across 22 U.S. states.

    Product
    La Mexicana Garlic Salsa 16 oz. Gourmet Style Garlic 16 oz.
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Drugs)·D-0071-2019·2018-10-24

    CeraVe Healing Lip Balm Recalled for Staphylococcus Aureus Contamination

    Product Quest Manufacturing LLC is recalling CeraVe Healing Lip Balm/SPF 30 due to failed microbiological testing for Staphylococcus aureus.

    Product
    CeraVe Healing Lip Balm/SPF 30 (avobenzone 3%, dimethicone 1%, homosalate 10%, octisalate 5%, octocrylene 10%, Net Wt. 0.15 oz. (4.25 g) stick, CeraVe LLC., New York, NY 10001, UPC 3 01872 49201 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0039-2019·2018-10-24

    Harmon Face Values Saline Nasal Gel Recalled for Quality Deviations

    Product Quest Manufacturing LLC is recalling Harmon Face Values Saline Nasal Gel with Soothing Aloe due to manufacturing deviations that could impact product quality.

    Product
    Harmon Face Values, Saline Nasal Gel with Soothing Aloe, 0.5 oz. (14.1 g) tube, Distributed by: Harmon Stores, Inc., Union, NJ 07083 USA, UPC 7 27510 00474 7 .
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0027-2019·2018-10-24

    Dermatone Sunscreen Stick Recalled for Staphylococcus Aureus Contamination

    Product Quest Manufacturing LLC is recalling Dermatone No-Touch Sunscreen Sticks because samples tested positive for Staphylococcus aureus.

    Product
    DERMATONE (titanium oxide 6% and zinc oxide 4.7%) No-Touch Sunscreen Stick, SPF 50, Net Wt. 0.49 oz. (13.9g) stick, Distributed by: Beaumont Products, Inc. Kennesaw, GA 30144, UPC 0 20908 05100 3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0103-2019·2018-10-24

    Thoratec CentriMag Motor Recall Due to Electrical Cable Failure

    Thoratec is recalling CentriMag Motors because a wire break or short circuit in the cable can cause the motor to stop.

    Product
    Thoratec CentriMag Motor, Model: 102956, a component of the Thoratec CentriMag Blood Pumping System and PediMag Blood Pumping System.
    Category
    Medical Device
    Distribution
    43 states