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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26951–26975 of 39747

  • SevereNHTSA·15V539000·2015-08-24

    East Manufacturing Recalls 2014-2016 Trailers Due to Wheel Bearing Fire Risk

    East Manufacturing is recalling 2014-2016 trailers because insufficient grease in wheel hubs may cause overheating, leading to fire or wheel detachment.

    Product
    EAST MANUFACTURING — EAST MANUFACTURING FRAME GENESIS TRAILER, DUMP TRAILER, FRAMELESS GENESIS TRAILER, REFUSE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V538000·2015-08-24

    McNeilus Recalls 2014-2015 CNG Trucks Due to Pressure Relief Defect

    McNeilus is recalling 2014-2015 CNG Refuse and Concrete trucks because pressure relief devices may fail to vent pressure, increasing the risk of tank explosion, fire, and injury.

    Product
    MCNEILUS — MCNEILUS CNG REFUSE TRUCK, CNG CONCRETE TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V535000·2015-08-21

    Strick Van Trailer Recall for Suspension Pivot Bolt Failure Risk

    Strick is recalling 2014 Van Trailers with SAF-Holland suspension systems because pivot bolts may fail, potentially causing the axle to separate from the trailer.

    Product
    STRICK — STRICK VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V532000·2015-08-20

    Oshkosh Recalls 2014-2015 S-Series Concrete Mixers Due to Pressure Relief Defect

    Oshkosh is recalling 2014-2015 S-Series concrete mixers powered by compressed natural gas because pressure relief devices may fail to vent pressure, posing a risk of tank explosion, fire, and injury.

    Product
    OSHKOSH — OSHKOSH S-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E067000·2015-08-20

    Reyco Granning Recalls Independent Front Suspension Assemblies for Loose Ball Joints

    Reyco Granning is recalling Independent Front Suspension assemblies manufactured between April 2011 and February 2015 due to loose ball joints that could separate and cause a loss of steering control.

    Product
    SUSPENSION:FRONT:CONTROL ARM:LOWER BALL JOINT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2961-2015·2015-08-19

    Bella Rosa Grated Parmesan Cheese Recalled for Undeclared Egg Lysozyme

    Arthur Schuman Inc. is recalling Bella Rosa Grated Parmesan Cheese because it may contain undeclared egg lysozyme, a potential allergen.

    Product
    Bella Rosa Parmesan Net Wt. 20 oz (567 g) 1.25 LB Arthur Schuman, Inc. Fairfield, NJ 07064 UPC 088231410041
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1328-2015·2015-08-19

    Methotrexate Injection Recalled Due to Presence of Particulate Matter

    Mylan Institutional LLC is recalling Methotrexate Injection vials due to the presence of particulate matter.

    Product
    Methotrexate Injection, USP 50 mg/2 mL (25 mg/mL), 2 mL Single-dose Vial, packaged in 5 x 2 mL vials per carton, Rx only, labeled as a) Distributed by Pfizer Labs, Division of Pfizer Inc., New York, NY 10017, NDC 0069-0146-01; and b) Manufactured for: Mylan Institutional LLC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2960-2015·2015-08-19

    Patel Grocery Coriander Powder Recalled for Undeclared Peanut Allergen

    Patel Grocery Corp is recalling America's Best Coriander Powder in New York due to undeclared peanut allergens.

    Product
    AMERICA'S BEST CORRIANDER POWDER, NET WT.: 1) 7 OZ, 2) 14 OZ. (400 GMS) and 3) 28 OZ, sealed in plastic bags, Packed by Patel Grocery 5303 4th Ave. Brooklyn, NY 11220
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2358-2015·2015-08-19

    Invacare Pronto Air Power Wheelchair Recall for Battery Overheating Risk

    Invacare is recalling 1,057 Pronto Air power wheelchairs because the batteries may overheat during charging, posing risks of chemical burns and property damage.

    Product
    Invacare¿ Pronto¿ Air Personal Transporter (power wheelchair), Invacare Corporation, One Invacare Way, Elyria, Ohio, 44035-4190, (800) 333 -6900.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2323-2015·2015-08-19

    Alcon ReSTOR Intraocular Lenses Recalled for Post-Operative Inflammation Reports

    Alcon Research, Ltd. is recalling ReSTOR intraocular lenses manufactured for Japan due to reports of post-operative inflammation and toxic anterior segment syndrome (TASS). No US distribution occurred.

    Product
    ReSTOR intraocular lens and ReSTOR Toric intraocular lens. The Alcon AcrySof IQ ReSTOR and IQ ReSTOR Toric intraocular lenses are posterior chamber lenses intended as optical implants designed to replace the human crystalline lens in adult patients following cataract surgery.…
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-2952-2015·2015-08-19

    D & D Foods Recalls Dijon Mustard Potato Salad for Allergen Mislabeling

    D & D Foods is recalling 110 cases of Dijon Mustard Potato Salad sold in Hy-Vee stores because the product contains milk and wheat but fails to disclose these allergens.

    Product
    Dijon Mustard Potato Salad, NET WT 3 LB (1.36 kg)
    Category
    Food
    Distribution
    8 states
  • SevereCPSC·15748·2015-08-19

    Grizzly Recalls 10-Inch Hybrid Table Saws Due to Laceration Hazards

    Grizzly Industrial is recalling 10-inch hybrid table saws because a loose motor pulley can strike the blade, causing metal fragments to fly and injure users.

    Product
    Grizzly 10-inch hybrid table saws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2950-2015·2015-08-19

    Lion Pavilion Tasty Peach Slices Recalled for Undeclared Sulfites

    Lion Pavilion Ltd. is recalling Tasty Peach Slices due to undeclared sulfites detected by New York State authorities.

    Product
    Tasty Peach Slices, NET WT. 3.87 OZ (110g), UPC 6 949663 601787 -- Product of China --- The product was packed in a clear plastic bottle/jar. --- 12.75 mg sulfites per serving.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-2956-2015·2015-08-19

    FDA Recalls Maxam Products for Unapproved Drug Claims

    James G. Cole, Inc. is recalling all Maxam brand products nationwide because they are misbranded, adulterated, and unapproved new drugs.

    Product
    ALL MAXAM PRODUCTS: The Maxam product is used orally in spray form and bears the Maxam label. ********The List of MAXAM products********************************************** AD Nutritional Support for a Positive Outlook; AFX Nutritional Support for Healthy Cellular…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1329-2015·2015-08-19

    Mylan Recalls Cytarabine Injection Vials Due to Particulate Matter

    Mylan Institutional LLC is recalling 8,340 vials of Cytarabine Injection due to the presence of particulate matter. The affected product was distributed nationwide.

    Product
    Cytarabine Injection 100 mg/5 mL (20 mg/mL), 5 mL Single-Dose Vial (NDC 0069-0152-01), packaged in 10 x 5 mL Vials per carton (NDC 0069-0152-02), Rx only, Distributed by Pfizer Labs, Division of Pfizer Inc., New York, NY 10017.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2373-2015·2015-08-19

    Fresenius Medical Care Recalls Naturalyte Liquid Bicarbonate Concentrate

    Fresenius Medical Care is recalling Naturalyte Liquid Bicarbonate Concentrate due to potential bacterial contamination. The recall covers 2,264,028 units distributed nationwide.

    Product
    Naturalyte Liquid Bicarbonate Concentrate 6.4 liter bottle A Dialysate Concentrate for Hemodialysis (liquid) Product Code: 08-4000-LB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V527000·2015-08-18

    Starcraft Transit Bus Recall for Fire Risk from Wiring

    Forest River is recalling 32 Starcraft transit buses due to an improperly routed cable that may cause an electrical short and fire.

    Product
    STARCRAFT BUS — STARCRAFT BUS ALL STAR XL, XLT, ALL STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V529000·2015-08-18

    E-One Emergency Vehicles Recalled for Lighting and Siren Safety Defect

    E-One is recalling 2013-2016 Pumpers, Tankers, and Rescue vehicles because the master power switch does not link to the start circuit, allowing operation without lights or sirens.

    Product
    E-ONE — E-ONE RESCUE, TANKER, PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V523000·2015-08-17

    Volvo Recalls 2012-2016 VAH Trucks for Steering Drag Link Defect

    Volvo is recalling 2012-2016 VAH trucks because a damaged steering component may corrode, potentially causing loss of steering and increasing crash risk.

    Product
    VOLVO — VOLVO VAH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V521000·2015-08-17

    Mack Pinnacle Trucks Recalled for Brake Chamber Mounting Defect

    Mack is recalling 2013-2015 Pinnacle trucks because incorrectly mounted brake chambers may contaminate calipers, increasing stopping distance and crash risk.

    Product
    MACK — MACK PINNACLE (CXU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V524000·2015-08-17

    Volvo Recalls 2012-2015 VNL and VNM Trucks for Brake Handle Defect

    Volvo is recalling 2012-2015 VNL and VNM trucks because the trailer hand brake handle may not return to the off position, potentially causing wheel overheating, fire, or tire blowout.

    Product
    VOLVO — VOLVO VNL, VNM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·112-2015·2015-08-17

    Givaudan Recalls Beef Tallow Products Produced Without Import Inspection

    Givaudan Flavors Corporation is recalling approximately 3,950 pounds of beef tallow products produced in Australia that were not inspected at the U.S. point of entry.

    Product
    Givaudan Flavors Corporation Recalls Beef Tallow Products Produced Without Benefit of Import Inspection
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·15V517000·2015-08-14

    Chrysler Recalls 2014-2015 Ram 1500 Diesel Trucks for Fire Risk

    Chrysler is recalling 2014-2015 Ram 1500 diesel trucks because a battery harness may rub against the frame, causing an electrical short that could lead to stalling or fire.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide