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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27101–27125 of 39749

  • CriticalFDA (Drugs)·D-1211-2015·2015-07-15

    Baxter Recalls Lactated Ringers Bags Due to Metal Particulate Matter

    Baxter Healthcare is recalling specific lots of Lactated Ringers Injection due to the presence of metal particulate matter.

    Product
    LACTATED RINGERS — LACTATED RINGERS (SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM LACTATE AND CALCIUM CHLORIDE)
    Category
    Drug
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-1210-2015·2015-07-15

    Baxter Recalls 10% Dextrose Injection Bags Due to Metal Particulate Matter

    Baxter Healthcare is recalling 18,324 bags of 10% Dextrose Injection due to the presence of metal particulate matter. The affected products were distributed in the US, Puerto Rico, and Bermuda.

    Product
    DEXTROSE — DEXTROSE (DEXTROSE MONOHYDRATE)
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1216-2015·2015-07-15

    Hospira Recalls Bupivacaine Hydrochloride Vials Due to Particulate Matter

    Hospira is recalling Bupivacaine Hydrochloride Injection vials because they contain free-floating and embedded iron oxide particles.

    Product
    BUPIVACAINE HYDROCHLORIDE — BUPIVACAINE HYDROCHLORIDE (BUPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E060000·2015-07-15

    Flex-A-Lite Recalls Electric Fan Kits Due to Fire Risk

    Flex-A-Lite is recalling specific electric fan kits because missing fuse holders and insufficient circuit breakers may cause electrical damage and vehicle fires.

    Product
    ENGINE AND ENGINE COOLING:COOLING SYSTEM:FAN recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2816-2015·2015-07-15

    Garden Fresh Potato Salad Kit Recalled for Listeria Risk

    Garden-Fresh Foods is recalling Steakhouse Potato Salad Kits after one case tested presumptive for Listeria monocytogenes. The product was distributed in Illinois.

    Product
    Garden Fresh Steakhouse Potato Salad Kit, CODE#1076, NET WT 10.75 LBS (4.876 KG) , UPC 0 01 11596 51076 4.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1989-2015·2015-07-15

    Alliance Partners Recalls Nakoma-SL Cervical Plating Drill Guides

    Alliance Partners LLC is recalling 21 Nakoma-SL Anterior Cervical Plating System drill guides because screws may advance through the plate during implantation.

    Product
    Nakoma-SL Anterior Cervical Plating System's Variable Single Barrel Drill Guide Product Usage: The Nakoma-SL ACP System is intended for anterior intervertebral screw fixation of the cervical spine at levels C2-T1. The Nakoma ACP System is indicated for temporary…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·101-2015·2015-07-15

    Aspen Foods Recalls Frozen Raw Stuffed Chicken Due to Salmonella Risk

    Aspen Foods is recalling approximately 1.98 million pounds of frozen, raw, stuffed, and breaded chicken products due to possible Salmonella Enteritidis contamination linked to illnesses in Minnesota.

    Product
    Aspen Foods Recalls Frozen, Raw, Stuffed & Breaded Chicken Products Due to Possible Salmonella Enteritidis Contamination
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2046-2015·2015-07-15

    Biomet Recalls A.L.P.S. Foot Locking Calcaneus Plates Due to Thread Defects

    Biomet is recalling 75 A.L.P.S. Foot Locking Calcaneus Plates because thread defects may cause screws to back out or shear, potentially requiring revision surgery.

    Product
    A.L.P.S. Foot Locking Calcaneus Plate,Small-Right. Provides the orthopaedic surgeon a means of bone fixation and helps generally in the management of fractures and reconstructive surgeries.
    Category
    Medical Device
    Distribution
    10 states
  • SevereFDA (Food)·F-2818-2015·2015-07-15

    Popcorn Factory Recalls Dill Pickle Popcorn Due to Undeclared Milk Allergen

    The Popcorn Factory is recalling Dill Pickle Lite Works Popcorn because it contains milk, an allergen not declared on the label.

    Product
    Dill Pickle Lite Works Popcorn , lot number 15111, packaged in a 4 oz foil white bag with black and green lettering.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-2788-2015·2015-07-15

    Kerry Foods Recalls Nondairy Creamer Due to Potential Metal Fragments

    Kerry Foods is voluntarily recalling specific lots of nondairy creamer produced in May 2015 due to the potential presence of small metal pieces from a broken production screen.

    Product
    Kraft French Vanilla, Creamer, Non-Dairy Creamer, Net WT/Contenido Neto 35.3 oz (1 kg) SKU 2100002971. Publix, Nondairy, FrenchVanilla, Naturally and Artificially Flavored Coffee Creamer, Net Wt 15 oz (425 g), SKU 4141501625.
    Category
    Food
    Distribution
    3 states
  • SevereCPSC·15182·2015-07-15

    Cooper Lighting Recalls Fluorescent Fixtures Due to Fire Hazard

    Cooper Lighting is recalling about 1.62 million fluorescent fixtures because the sockets can overheat, arc, and melt, posing a fire hazard.

    Product
    Cooper Lighting, Portfolio and Utilitech fluorescent lighting fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1950-2015·2015-07-15

    Shiley Neonatal and Pediatric Tracheostomy Tubes Recalled for Breathing Difficulties

    FDA is recalling Shiley Neonatal and Pediatric Tracheostomy Tubes because patients reported discomfort and breathing difficulties after switching to these products.

    Product
    Shiley Neonatal, Pediatric and Long Pediatric Tracheostomy Tube, Cuffless. Model Numbers…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2841-2015·2015-07-15

    Brown Betty Coconut Milk Powder Mix Recalled for Undeclared Milk Allergen

    Bedessee Imports is recalling Brown Betty Coconut Milk Powder Mix because it contains sodium caseinate but lacks a milk declaration.

    Product
    Bedessee Brown Betty BRAND COCONUT MILK Powder Mix, NET WT: 1) 1.76 OZ (50 g) and 2) 10.6 OZ. IMPORTED BY BEDESSEE IMPORTS LTD. Brooklyn, NY USA 11208. PRODUCT OF VIETNAM.
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Drugs)·D-1089-2015·2015-07-15

    Teva Recalls Adrucil Fluorouracil Injection Due to Particulate Matter

    Teva Pharmaceuticals is recalling Adrucil (fluorouracil injection) vials due to the presence of black particulate matter, including silicone rubber and drug crystals.

    Product
    Adrucil (fluorouracil injection, USP) Pharmacy Bulk Package Not for Direct Infusion, 5 g/100 mL (50 mg/mL), For Intravenous Use Only, Rx Only, Teva Parenteral Medicines, Inc., Irvine, CA 92618, NDC 0703-3019-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E058000·2015-07-14

    Agility Fuel Systems Recalls CNG Fuel Systems Due to Pressure Relief Defect

    Agility Fuel Systems is recalling certain compressed natural gas (CNG) fuel systems because pressure relief devices may fail to vent pressure, increasing the risk of tank explosion, fire, and injury.

    Product
    FUEL SYSTEM, OTHER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E059000·2015-07-14

    Emcara Pressure Relief Devices Recalled for CNG Tank Explosion Risk

    Emcara is recalling specific Pressure Relief Devices (PRDs) that may fail to vent pressure, potentially causing CNG tank explosions, fire, and injury.

    Product
    FUEL SYSTEM, OTHER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15T011000·2015-07-13

    Hercules Recalls All Trac A/T Tires Due to Tread Separation Risk

    Hercules Tire & Rubber Company is recalling approximately 90,000 All Trac A/T tires because the tread may separate, increasing the risk of a vehicle crash.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·096-2015·2015-07-12

    Barber Foods Recalls Stuffed Chicken Products Due To Salmonella Risk

    Barber Foods is recalling approximately 1.7 million pounds of frozen, raw stuffed chicken products that may be contaminated with Salmonella Enteritidis.

    Product
    AdvancePierre Foods, Inc. — Barber Foods Recalls Stuffed Chicken Products Due To Possible Salmonella Enteritidis Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V443000·2015-07-10

    Autocar Recalls 2015-2016 Xpeditor Vehicles Due to HVAC Fire Risk

    Autocar is recalling 1,042 model year 2015-2016 Xpeditor vehicles because the defrost mode door actuators in the HVAC units may overheat, increasing the risk of a fire.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V442000·2015-07-10

    GM Recalls 2014-2015 Chevrolet Cruze and Volt for Steering Defect

    General Motors is recalling specific 2014-2015 Chevrolet Cruze and 2015 Chevrolet Volt vehicles because the inner tie rod may not be tightened correctly, which could cause the tie rod to separate from the steering gear.

    Product
    CHEVROLET — CHEVROLET CRUZE, VOLT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V444000·2015-07-10

    Dodge Challenger Recall: Driver Air Bag Inflator Rupture Risk

    Chrysler is recalling 2008-2010 Dodge Challengers because the driver's air bag inflator may rupture during deployment, potentially causing serious injury or death.

    Product
    DODGE — DODGE CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V440000·2015-07-10

    Wilson Recalls 2006-2015 Grain Trailers Due to Kingpin Weld Failure Risk

    Wilson Trailer Company is recalling 2006-2015 Grain trailers because welds on the kingpin assembly may fail, potentially causing the trailer to detach from the tractor.

    Product
    WILSON — WILSON GRAIN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide