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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18326–18350 of 39605

  • SevereFDA (Drugs)·D-0718-2018·2018-05-02

    Coastal Meds Recalls ADENO-PLEX Injectable Due to Particulate Matter

    Coastal Meds, LLC. is recalling 200 vials of ADENO-PLEX Injectable-30 mL MDV due to the presence of unknown particulate matter.

    Product
    ADENO-PLEX Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1477-2018·2018-05-02

    Ion Beam Applications Recalls Proteus Proton Beam Therapy Systems

    Ion Beam Applications is recalling five Proteus proton beam therapy systems because a software error may cause under-irradiation or additional X-ray exposure.

    Product
    Proteus 235, ProteusPLUS or Proteus ONE produces and delivers a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation.
    Category
    Medical Device
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0702-2018·2018-05-02

    Premier Pharmacy Labs Recalls NeoStigmine Syringes Due to Sterility Concerns

    Premier Pharmacy Labs is recalling NeoStigmine Methylsulfate syringes because routine testing of other lots detected microbial contamination risks.

    Product
    NEOstigmine Methylsulfate (1 mg/mL) 3mg per 3mL. 3mL Single Dose Syringe. Premier Pharmacy Labs. 8265 Commercial Way Weeki Wachee, FL 34613 NDC 69623-234-14.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0723-2018·2018-05-02

    Coastal Meds Recalls LIPO-DEN PLUS Injectable Due to Particulate Matter

    Coastal Meds, LLC. is recalling 1,457 vials of LIPO-DEN PLUS Injectable because of the presence of unknown particulate matter. The product was distributed nationwide in the USA.

    Product
    LIPO-DEN PLUS Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0697-2018·2018-05-02

    Bayer Recalls Alka-Seltzer Plus Packages Due to Ingredient Label Mismatch

    Bayer is recalling specific Alka-Seltzer Plus packages because the ingredients listed on the front sticker may not match the actual product inside the carton.

    Product
    All Alka-Seltzer Plus¿ packages with a full front panel instant Redeemable Coupon (IRC) affixed to the individual carton. The recalled products can be identified by checking the Bayer logo located on the lower left corner of the front of the carton. If the logo has an orange or…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V282000·2018-05-01

    2018 Jeep Cherokee Recalled for Fuel Tube Leak Fire Risk

    Chrysler is recalling 2018 Jeep Cherokee vehicles with 2.4L engines because a fuel tube may leak, increasing the risk of a fire.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V279000·2018-05-01

    2018 Jeep Compass Recalled for Front Suspension Welding Defect

    Chrysler is recalling 2018 Jeep Compass vehicles because front lower control arms may be incorrectly welded, potentially causing separation and loss of vehicle control.

    Product
    JEEP — JEEP COMPASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V277000·2018-05-01

    RAM 4500 and 5500 Trucks Recalled for Brake Hose Corrosion Risk

    Chrysler is recalling 2018 RAM 4500 and 5500 trucks because brake hose ferrules may lack anti-corrosion plating, potentially causing fluid leaks and loss of braking.

    Product
    RAM — RAM 4500, 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V280000·2018-05-01

    Chrysler Recalls 2018 Vehicles for Incorrect Transmission Park Lock Rod

    Chrysler is recalling 2018 Dodge, Jeep, Chrysler, and RAM vehicles because an incorrect transmission park lock rod may prevent the vehicle from staying in Park, increasing crash risk.

    Product
    DODGE — DODGE, CHRYSLER, JEEP CHARGER, CHALLENGER, DURANGO, 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V281000·2018-05-01

    Dodge Charger Recall: Front Driveshaft May Detach and Cause Crash

    Chrysler is recalling 2015-2018 Dodge Charger pursuit police vehicles because the front driveshaft may detach, creating a road hazard and increasing crash risk.

    Product
    DODGE — DODGE CHARGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V275000·2018-04-30

    Ford Recalls 2015-2017 Transit Vehicles for Electrical Wiring Fire Risk

    Ford is recalling 25,658 2015-2017 Transit vehicles with trailer tow modules because water intrusion can corrode wiring, potentially causing electrical shorts, fires, or crashes.

    Product
    FORD — FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·034-2018·2018-04-28

    Pinnacle Foods Recalls Beef Products Due to Possible Processing Deviation

    Pinnacle Foods Inc. is recalling approximately 32,479 pounds of heat-treated, shelf-stable beef products due to a possible processing deviation that may have led to toxin contamination.

    Product
    Pinnacle Foods Inc. Recalls Beef Products Due to Possible Processing Deviation
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V272000·2018-04-27

    Mercedes-Benz Recalls SUVs for Active Curve System Fire Risk

    Mercedes-Benz is recalling specific 2012-2017 SUVs because oil in the Active Curve System may leak and cause a fire if the level is low.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG ML63, GL350, GL450, GL550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V273000·2018-04-27

    Smart Fortwo Recall: Rear Insulation Mat Fire Risk

    Mercedes-Benz is recalling 2008-2009 Smart Fortwo vehicles because a rear insulation mat may contact hot exhaust components, increasing fire risk.

    Product
    SMART — SMART FORTWO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V269000·2018-04-27

    Forest River Recalls 2018 Starcraft and Glaval Buses for Gear Shift Defect

    Forest River is recalling 2018 Starcraft Bus XLT and Glaval Bus Concorde II models because a gear shift cable clip may not be properly seated, potentially causing the vehicle to roll or shift unexpectedly.

    Product
    GLAVAL BUS — GLAVAL BUS, STARCRAFT BUS CONCORDE II, XLT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E027000·2018-04-27

    Advance Stores Recalls ToolWorks TW1489 Fuse Kits for Fire Risk

    Advance Stores is recalling ToolWorks TW1489 Fuse Kits sold at Advance Auto Parts and Carquest because the fuses may fail to protect circuits, increasing fire risk.

    Product
    ELECTRICAL SYSTEM:WIRING:FUSES AND CIRCUIT BREAKERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E025000·2018-04-26

    ZF Axle Brake Caliper Guide Pin Recall

    ZF North America is recalling certain axles with radial air disk brakes because a broken guide pin support bolt may cause loss of braking ability or tire pressure.

    Product
    SERVICE BRAKES, AIR:DISC:CALIPER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1383-2018·2018-04-25

    Nutrizone Recalls Nirvanio Green Malay Kratom Due to Salmonella Risk

    Nutrizone LLC is recalling all packages of Nirvanio Green Malay Kratom because dietary supplements have the potential to be contaminated with Salmonella.

    Product
    Nirvanio Green Malay Kratom all packages, all quantities
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1119-2018·2018-04-25

    Club 13 Kratom Maeng Da Red Powder Recalled for Salmonella

    Club 13 Enterprises Warehouse is recalling specific lots of Maeng Da Red powder after testing confirmed the presence of Salmonella.

    Product
    Club 13 Kratom Maeng Da Red powder; Pouches of 15, 30, 90, 150, 454 grams, and Club 13 Kratom Maeng Da Red powder in bulk bags.
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1111-2018·2018-04-25

    Aspire Food Group Recalls EXO Cricket Protein Bars for Undeclared Sulfites

    Aspire Food Group is recalling EXO Cricket Protein Bars in Blueberry Vanilla flavor because they contain undeclared sulfites. The recall affects 40,512 units distributed in the United States and Germany.

    Product
    EXO Cricket Protein Bar Blueberry Vanilla; Net Wt 2.1 Oz. packaged in a film wrapper, 12 units per case; UPC: 861703000069
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1117-2018·2018-04-25

    Global Commodities Recalls Frozen Grated Coconut Due to Salmonella

    Global Commodities Corp. is recalling one lot of frozen grated coconut after the California Department of Public Health detected Salmonella.

    Product
    Buenas Grated coconut - frozen; Kinayod na Niyog Noix de Coco Rape; UPC: 4806514650443 Keep Frozen Net Wt. 16 oz., (4545 g) plastic bag Product of the Philippines Ingredients: Grated coconut Meat (95%) Water and preservative: Sodium Benzoate.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1108-2018·2018-04-25

    Davis Chocolate Peanut Morsels Recalled for Listeria Contamination

    Davis Chocolate is voluntarily recalling peanut morsels and organic peanut chips due to Listeria monocytogenes detected by a customer's laboratory analysis.

    Product
    Davis Chocolate Peanut Morsels /Organic Peanut Chips
    Category
    Food
    Distribution
    1 state