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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18301–18325 of 39605

  • SevereNHTSA·18V295000·2018-05-03

    GM Recalls 2014-2017 Chevrolet Express and GMC Savana for Fire Risk

    General Motors is recalling 2014-2017 Chevrolet Express and GMC Savana vans because liquid leakage in the driver's window switch can cause corrosion and increase the risk of a fire.

    Product
    GMC — GMC, CHEVROLET SAVANA, EXPRESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V287000·2018-05-03

    Porsche Recalls 2015 918 Spyder for Rear Suspension Control Arm Defect

    Porsche is recalling 2015 918 Spyder vehicles because rear suspension connecting shafts may fail due to stress corrosion cracking, increasing the risk of a crash.

    Product
    PORSCHE — PORSCHE 918 SPYDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V286000·2018-05-03

    Jayco Recalls 2018 Eagle Fifth Wheel Trailers Due to Pin Box Defect

    Jayco is recalling 2018 Eagle HT fifth wheel trailers because a spindle placement error in the pin box may cause the bearing to become loose, increasing the risk of a crash.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V290000·2018-05-03

    Navistar Recalls 2019 IC Bus CE School Buses Due to Brake Line Routing

    Navistar is recalling 2019 IC Bus CE school buses because an improperly routed air supply line may cause unintentional parking brake modulation, increasing crash risk.

    Product
    IC BUS — IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V288000·2018-05-03

    Daimler Recalls 2017 Sprinter Vans for Missing Structural Welds

    Daimler Vans USA is recalling 2017 Mercedes-Benz and Freightliner Sprinter 2500 and 3500 vans because missing spot welds may reduce body strength in a crash.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1136-2018·2018-05-02

    Cheezwhse Recalls L 'Explorateur Soft Ripened Cheese for Listeria Risk

    Cheezwhse is recalling specific lots of L 'Explorateur soft ripened cheese due to potential Listeria monocytogenes contamination. The product was distributed in several US states and Washington D.C.

    Product
    Formagere de la Brie brand, l 'Explorateur, soft ripened cheese made from pasteurized milk, product comes in a 250g (8.8 oz), clear plastic package marked with lot # on the bottom, with UPC: 3 390010 004080.
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-1137-2018·2018-05-02

    Kitchen By The Sea Bloody Hell Mary Recalled for Allergen Mislabeling

    Kitchen By The Sea is recalling Bloody Hell Mary products because egg, soy, wheat, and sulfites are not listed on the labels.

    Product
    Bloody Hell Mary, HOT, Kitchen By The Sea, From the Beach House, Net Wt. 32 oz. (.9L), Low Sodium
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1410-2018·2018-05-02

    Rose Acre Farm Shell Eggs Recalled for Salmonella Braenderup Risk

    Rose Acre Farm is recalling shell eggs due to potential Salmonella Braenderup contamination. The recall affects direct consignees in 13 states.

    Product
    Shell Eggs packaged in quantities and styles of pack (plastic and pulp cartons, flats, and boxes)
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Drugs)·D-0719-2018·2018-05-02

    Coastal Meds Recalls Hydroxocobalamin Injectable Due to Particulate Matter

    Coastal Meds, LLC. is recalling 1,506 vials of Hydroxocobalamin Injectable due to the presence of unknown particulate matter. The product was distributed nationwide.

    Product
    HYDROXOCOBALAMIN Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1127-2018·2018-05-02

    Seabear Recalls Cold Smoked Coho Salmon Lox Due to Salt Deviations

    Seabear Company is recalling 2,080 units of Cold Smoked Wild Coho Salmon Lox due to water phase salt deviations and mislabeled storage instructions.

    Product
    Cold Smoked Wild Coho Salmon Lox , Gerard & Dominique Seafoods brand, Reduced Oxygen Packaging, Net Wt. 3 oz (85g). UPC 7 52047 92635 4. The package label of the Cold Smoked Coho Salmon bears this instructions "***KEEP REFRIGERATED AT OR BELOW 38 F***". The master case…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0699-2018·2018-05-02

    Premier Pharmacy Labs Recalls Morphine Sulfate Injection Due to Sterility Concerns

    Premier Pharmacy Labs is recalling specific lots of Morphine Sulfate Injection because routine testing of other lots detected microbial contamination risks.

    Product
    Morphine Sulfate 2 mg/mL PF Injection. 1 mL in a 3ml Sterile Single-Dose Syringe. 8265 Commerical Way Weeki Wachee, FL 34613. NDC 69623-129-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0726-2018·2018-05-02

    Coastal Meds Recalls Pyridoxine Injectable Due to Particulate Matter

    Coastal Meds, LLC. is recalling 635 vials of Pyridoxine Injectable due to the presence of unknown particulate matter.

    Product
    PYRIDOXINE Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1134-2018·2018-05-02

    Nxtgen Botanicals Maeng Da Kratom Recalled for Salmonella Risk

    NGB Corp is recalling Nxtgen Botanicals Maeng Da Kratom dietary supplements due to potential Salmonella contamination.

    Product
    Nxtgen Botanicals, Maeng Da Kratom, Dietary Supplement, 70 capsules
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0724-2018·2018-05-02

    Coastal Meds Recalls LIPO-PLEX Injectable Due to Particulate Matter

    Coastal Meds, LLC. is recalling LIPO-PLEX Injectable-30 mL vials nationwide due to the presence of unknown particulate matter.

    Product
    LIPO-PLEX Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0700-2018·2018-05-02

    Premier Pharmacy Labs Recalls Morphine Sulfate Syringes Due to Sterility Concerns

    Premier Pharmacy Labs Inc is recalling 4,192 syringes of Morphine Sulfate 4 mg/mL PF Injection due to a lack of assurance of sterility.

    Product
    Morphine Sulfate 4 mg/mL PF Injection. 1 mL in a 3ml Sterile Single-Dose Syringe. 8265 Commerical Way Weeki Wachee, FL 34613. NDC 69623-127-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1532-2018·2018-05-02

    BD Vacutainer Push Button Blood Collection Set Recalled for Sterility Issues

    Becton Dickinson is recalling BD Vacutainer Push Button Blood Collection Sets because they do not meet the labeled sterility assurance level.

    Product
    BD Vacutainer¿ Push Button Blood Collection Set 0.8 x 19 mm x 305 mm 21G x ¿ x 12 Catalog 367344
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1138-2018·2018-05-02

    Kitchen by the Sea Recalls Bloody Mary Mix Due to Allergen Mislabeling

    Kitchen by the Sea is recalling Bloody Mary mix because the labels failed to list egg, soy, wheat, and sulfites.

    Product
    Bloody Mary, Medium, Kitchen by the Sea, From the The Beach House, Net Wt. 32.oz, Low Sodium
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·18V285000·2018-05-02

    Thor Motor Coach Recalls Tuscany and Venetian Motorhomes for Fire Risk

    Thor Motor Coach is recalling 2011-2017 Tuscany and Venetian motorhomes because an incorrectly routed power steering hose may cause electrical arcing and a fire.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH VENETIAN, TUSCANY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1126-2018·2018-05-02

    Seabear Hot Smoked Keta Salmon Recalled for Salt Deviations and Mislabeling

    Seabear Company is recalling 381 units of Hot Smoked Keta Beergarden Salmon due to water phase salt deviations and mislabeled storage instructions.

    Product
    Hot Smoked Keta Beergarden Salmon, Seabear brand, Reduced Oxygen Packaging, Net Wt. 4oz (113g). No UPC.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1118-2018·2018-05-02

    Whole Foods Recalls Undeclared Egg Allergen in Iced Easter Cookies

    Whole Foods Market is recalling decorated Easter cookies sold in nine Northern California locations because the signage failed to declare egg as an ingredient and allergen.

    Product
    Decorated (iced holiday cookies sold from self service cookie displays - cookies in the shape of eggs, bunnies and chicks. The signage by the displays do not declare egg as an ingredient of the cookies. Cookies are received in a 9 lb. bag Correct Ingredients: Unbleached…
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0701-2018·2018-05-02

    Premier Pharmacy Labs Recalls Hydromorphone Syringes Due to Sterility Concerns

    Premier Pharmacy Labs is recalling 3,570 hydromorphone syringes because routine testing of other lots found microbial contamination risks.

    Product
    Hydromorphone HCl 1 mg/mL PF INJ. 1mL in a 3mL Sterile Single-Dose Syringe. 8265 Commercial Way Weeki Wachee, FL 34613 NDC 69623-249-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V284000·2018-05-02

    Volkswagen Atlas Recall for Fuel Tank Leak Fire Risk

    Volkswagen is recalling 2018 Atlas vehicles because a manufacturing error may cause the fuel tank to leak, increasing the risk of a fire.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0722-2018·2018-05-02

    FDA Recalls Lipoderm Extreme Injectable Due to Particulate Matter

    Coastal Meds, LLC. is recalling 3,733 vials of LIPO-DEN EXTREME Injectable-30 mL due to the presence of unknown particulate matter.

    Product
    LIPO-DEN EXTREME Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide