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.

Filters

Agency

All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

24651–24675 of 39693

  • SevereFDA (Drugs)·D-0814-2016·2016-04-13

    Actavis Recalls Dextroamphetamine Tablets Due to Impurity Failures

    Actavis Elizabeth LLC is recalling 257,746 bottles of Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 20 mg, because they failed impurity specifications.

    Product
    Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 20 mg, 100 ct. bottle, Rx Only. Manufactured by: Actavis Elizabeth LLC, Elmora Avenue, Elizabeth, NJ 07207. Distributed by: Actavis, Inc., 80 Columbia Road, Bldg B…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1323-2016·2016-04-13

    MicroAire French Rasp Aspiration Cannula Recalled for Bending or Breaking

    MicroAire Surgical Instruments is recalling 37 units of the PAL-R4011XL French Rasp aspiration cannula because they bent or broke during surgery.

    Product
    MicroAire PAL-R4011XL - 40cm x 4 mm Del Vecchio French Rasp aspiration cannula
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1315-2016·2016-04-13

    ScottCare TeleSentry Battery Recall Due to Explosion Risk During Recharging

    ScottCare is recalling 9,067 TeleSentry batteries after a complaint that one exploded while recharging. The batteries are used in cardiac monitoring devices.

    Product
    TeleSentry Battery, 3.7 Li-Ion Polymer Battery, CAUTION Do not expose to high temperature. Do not disassemble. Dispose of properly. Use specified charger only. 60pC/140pF The ScottCare Corporation. Intended for diagnostic evaluation of patients who experience transient…
    Category
    Medical Device
    Distribution
    24 states
  • SevereFDA (Drugs)·D-0804-2016·2016-04-13

    Meditech Formula 9 Injection Recalled for Sterility Assurance Issues

    Meditech Laboratories is recalling Formula 9 Injection vials due to incomplete production data regarding sterility assurance.

    Product
    Formula 9 (Papaverine 0.9 mg, Phentolamine 0.1 mg, Atropine 0.01 mg, PGE 20 mcg/mL) Injection, 5 mL vial, Rx only, Meditech Laboratories, Inc., 3200 Polaris Ave., Suite 27, Las Vegas, NV 89102.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1037-2016·2016-04-13

    NutraKey Recalls VPro Raw Plant Protein Due to Undeclared Soy

    NutraKey, Inc. is recalling VPro Raw Plant Protein, Mocaccino, because it contains undeclared soy. The product was distributed nationwide.

    Product
    VPro Raw Plant Protein, Mocaccino. Packaged in a plastic bottle with green, white, and black adhesive label. Packaged in 1 lb (15 serving) and 2 lb (30 serving).
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0807-2016·2016-04-13

    Meditech Formula 0 Injection Recalled for Sterility Assurance Issues

    Meditech Laboratories is recalling Formula 0 Injection due to incomplete production data regarding sterility assurance.

    Product
    Formula 0 (PGE 20 mcg/mL) Injection, 5 mL vials, Rx only, Meditech Laboratories, Inc., 3200 Polaris Ave., Suite 27, Las Vegas, NV 89102.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0802-2016·2016-04-13

    Meditech Formula 2 Injection Recalled for Superpotent Drug Ingredient

    Meditech Laboratories is recalling Formula 2 Injection vials because one ingredient exceeded assay specifications, making the drug superpotent.

    Product
    Formula 2 (Papaverine 9 mg, Phentolamine 1 mg, Atropine 0.1 mg, PGE 10 mcg/mL) Injection, 5 mL vials, Rx only, Meditech Laboratories, Inc., 3200 Polaris Ave., Suite 27, Las Vegas, NV 89102.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1031-2016·2016-04-13

    Sweetwater Sprouts Recalled for Potential Salmonella Contamination

    Sweetwater Farms LLC is recalling sprouted alfalfa due to potential Salmonella contamination. The product was distributed in Arkansas, Kansas, and Oklahoma.

    Product
    Sweetwater Sprouts 100% Pure Sprouted Alfalfa packaged in the following configurations: 4 oz. plastic bags (UPC 7 56733 00104 2) packed 12 per case; 16 oz. (1 lb.) plastic bags; and 5 lb. bulk boxes The product is shipped in cardboard cases labeled with product and lot…
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·16V214000·2016-04-13

    Hillsboro Aluminum Utility Trailer Recall for Axle Hardware Defect

    Hillsboro is recalling 2016 aluminum utility trailers because improperly installed axle hardware may cause the axle to shift, increasing crash risk.

    Product
    HILLSBORO — HILLSBORO ALUMINUM UTILITY TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V206000·2016-04-12

    Freightliner Trucks Recalled for Rear Brake Caliper Installation Error

    Daimler Trucks North America is recalling 2010-2017 Freightliner trucks because incorrectly installed rear brake calipers may contact the suspension, reducing braking effectiveness.

    Product
    FREIGHTLINER — FREIGHTLINER 108SD, COLUMBIA, BUSINESS CLASS M2, 114SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·028-2016·2016-04-12

    Mountain Products Recalls Pork Products Due to Undeclared Allergens

    Mountain Products Inc. is recalling approximately 467 pounds of bacon and pork sausage products because they contain undeclared milk, soy, and wheat allergens.

    Product
    Mountain Products Inc. — Mountain Products Inc. Recalls Pork Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • SevereCPSC·16140·2016-04-12

    Coleman Recalls CTAC Lithium-Ion Flashlights Due to Fire Hazard

    Coleman is recalling about 8,500 CTAC lithium-ion flashlights sold in the U.S. because the batteries can overheat and catch fire.

    Product
    Coleman® CTAC Lithium-Ion Flashlights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V203000·2016-04-11

    Mazda Recalls CX-3, Mazda2, CX-5, and CX-9 for Steering Knuckle Defect

    Mazda is recalling specific 2013-2016 CX-3, Mazda2, CX-5, and CX-9 vehicles because front strut mounting bolts may loosen, potentially causing a loss of steering control.

    Product
    MAZDA — MAZDA CX-9, MAZDA2, CX-5, CX-3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V202000·2016-04-11

    Ram ProMaster City Recall for Electrical Harness Water Intrusion

    Chrysler is recalling 2015-2016 Ram ProMaster City vans because a low-voltage electrical harness connector may corrode, causing the transmission to unexpectedly shift into neutral.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V193000·2016-04-07

    Nissan Recalls 2016 Maxima and Murano for Brake System Defect

    Nissan is recalling 2016 Maxima and Murano vehicles because a damaged O-ring in the ABS actuator may reduce brake fluid pressure, increasing crash risk.

    Product
    NISSAN — NISSAN MAXIMA, MURANO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V198000·2016-04-07

    Toyota Recalls 2016 RAV4, Lexus RX350, and ES350 for Brake Defect

    Toyota is recalling 2016 RAV4, Lexus RX350, and ES350 vehicles because a damaged O-ring in the ABS actuator may cause improper brake fluid pressure control, increasing crash risk.

    Product
    LEXUS — LEXUS, TOYOTA RX350, RAV4, ES350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·027-2016·2016-04-07

    Pilgrim's Pride Recalls Chicken Nuggets Due to Plastic Contamination

    Pilgrim's Pride is recalling fully cooked chicken nuggets that may contain plastic. No illnesses have been reported.

    Product
    Pilgrim's Pride Corporation — Pilgrim's Pride Corp. Recalls Poultry Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    13 states
  • SevereCPSC·16138·2016-04-07

    GolfBuddy GPS Bands Recalled by Deca International Due to Burn Hazard

    Deca International is recalling GolfBuddy BB5 GPS bands because charging ports can produce an electrical charge that burns exposed skin. Two consumer burn reports have been received.

    Product
    GolfBuddy golf GPS bands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0902-2016·2016-04-06

    Lipari Foods Recalls Fancy Fruit & Nut Mix Due to Salmonella Risk

    Lipari Foods, Inc. is recalling Fancy Fruit & Nut Mix products because they may be contaminated with Salmonella.

    Product
    Fancy Fruit & Nut Mix 9-oz. retail plastic tub or 25-lb. bulk plastic bag. 12, 9-oz. tubs per case. 1, 25-lb. bag per case.
    Category
    Food
    Distribution
    14 states
  • CriticalFDA (Food)·F-1004-2016·2016-04-06

    Heritage International Recalls Trader Joe's Raw Cashew Pieces for Salmonella

    Heritage International is recalling Trader Joe's Raw Cashew Pieces due to potential Salmonella contamination. The product was distributed to specific U.S. Trader Joe's locations.

    Product
    Trader Joe's Nuts Raw Cashew Pieces NET Wt. 18 oz (1 LB) UPC Code: 0050 5154 Product of Thailand, Vietnam, & India Packaged in Thailand
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0817-2016·2016-04-06

    Kanan Enterprises Recalls Pistachios Due to Potential Salmonella Contamination

    Kanan Enterprises is recalling Favorites Natural Pistachios because the supplier notified them the product may contain Salmonella. The recall affects 408 cases distributed to five states.

    Product
    Favorites Natural Pistachios, roasted & salted, 4.5 oz (128g) pouch UPC 0 38445 12286 5 Proudly distributed by Circle K Stores, Inc. P.O. Box 52085 Phoenix, AZ 85072 www.circlek.com
    Category
    Food
    Distribution
    5 states