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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17901–17925 of 39605

  • SevereFDA (Devices)·Z-2151-2018·2018-06-20

    Sun Med Recalls Adult Manual Resuscitators Due to Port Detachment Risk

    Sun Med, LLC is recalling 55 cases of Medline Adult Manual Resuscitators because the patient port retaining ring may not fully seat, potentially detaching the port and impacting air delivery.

    Product
    MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK 5, BAG RESERVOIR, PEEP VALVE AND 7 FT. OXYGEN TUBING, REF CPRM1116PD5
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2208-2018·2018-06-20

    Angiodynamics Recalls RS 5F DL BIOFLO PASV Kits Due to Endotoxins

    Angiodynamics Inc. is recalling 7 boxes of RS 5F DL BIOFLO PASV kits because components may contain unsafe levels of bacterial endotoxins.

    Product
    RS 5F DL BIOFLO PASV, Catalog Number 60M150373
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Food)·F-1555-2018·2018-06-20

    Hill Country Fare Neapolitan Ice Cream Recalled for Metal Pieces

    H-E-B is recalling Hill Country Fare Neapolitan ice cream in Texas and Mexico because it may contain broken metal pieces.

    Product
    Hill Country Fare Neopolitan 4.5 quarts and 56 ounces; Hill Country Fare Neopolitan (Mexico) 4.5 quarts
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2227-2018·2018-06-20

    Seaberg SAM XT-C Tourniquet Recall Due to Potential Buckle Failure

    The Seaberg Company is recalling SAM XT-C tourniquets because internal testing showed stitches securing the buckle might fail, posing a risk of serious injury or death.

    Product
    Part #: SAM XT-C, Model: Hi-Viz Orange or Civilian
    Category
    Medical Device
    Distribution
    23 states
  • SevereFDA (Devices)·Z-2159-2018·2018-06-20

    Maquet Aortic Arterial Cannula Recalled for De-airing Plug Breakage Risk

    Maquet Cardiopulmonary Ag is recalling specific lots of Aortic Arterial Cannulas because the de-airing plugs may break during removal.

    Product
    Aortic Arterial Cannula 20 Fr (O.D.); 23 cm (L); with 3/8-inch wide connector, Part Number 701002206, Article Number A20-0101. For use in cardiopulmonary bypass
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2188-2018·2018-06-20

    Angiodynamics Recalls XCELA PASV Nitinol Wire Kits Due to Endotoxin Risk

    Angiodynamics Inc. is recalling 7 boxes of XCELA PASV 5F SL 55CM IR-145 Nitinol Wire Kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    XCELA PASV 5F SL 55CM IR-145 Nitinol Wire KIT PG, Catalog Number 25-124
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2146-2018·2018-06-20

    Sun Med Recalls Adult Manual Resuscitators Due to Port Detachment Risk

    Sun Med, LLC is recalling 1,742 cases of Medline Adult Manual Resuscitators because the patient port retaining ring may not fully seat, potentially allowing the port to detach during use and impacting air delivery.

    Product
    MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, BAG RESERVOIR AND 7 FT. OXYGEN TUBING, REF CPRM1116
    Category
    Medical Device
    Distribution
    2 states
  • SevereNHTSA·18E042000·2018-06-19

    Bosch High Pressure Fuel Pump Recall for Fire Risk

    Bosch is recalling high pressure fuel pump assemblies for Ford and GM vehicles because welds may fracture, causing a fuel leak that could lead to a fire.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18V402000·2018-06-15

    Mazda Recalls Vehicles Due to Passenger Air Bag Inflator Explosion Risk

    Mazda is recalling specific 2003-2011 models because passenger air bag inflators may explode during deployment, potentially causing serious injury or death.

    Product
    MAZDA — MAZDA RX-8, MAZDASPEED6, MAZDA6, MPV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18V404000·2018-06-15

    Mazda Recalls MPV and RX-8 Vehicles for Air Bag Inflator Defect

    Mazda is recalling 2005-2006 MPV and 2005-2009 RX-8 vehicles because the passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.

    Product
    MAZDA — MAZDA MPV, RX-8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18V403000·2018-06-15

    Mazda Recalls 2009-2010 RX-8 Vehicles for Air Bag Inflator Defect

    Mazda is recalling 2009-2010 RX-8 vehicles because the passenger air bag inflator may explode during deployment, posing a risk of serious injury or death.

    Product
    MAZDA — MAZDA RX-8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V410000·2018-06-15

    2017-2018 Thomas Built Buses Saf-T-Liner EFX Air Brake Recall

    Daimler Trucks North America is recalling 2017-2018 Thomas Built Buses Saf-T-Liner EFX transit buses due to a check valve defect that may cause sudden parking brake activation and increase crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E041000·2018-06-15

    Simard Suspensions Recalls Front Axles Due to Wheel Detachment Risk

    Simard Suspensions is recalling certain front suspensions because heat from brakes may melt plastic insulators, causing wheels to detach and increasing crash risk.

    Product
    SUSPENSION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V407000·2018-06-15

    Mercedes-Benz Recalls 2018 S-Class Vehicles for Electrical Fire Risk

    Mercedes-Benz is recalling 2018 S-Class and Maybach vehicles because improperly secured electrical power bars in the trunk may increase the risk of a fire or loss of vehicle functions.

    Product
    MERCEDES-MAYBACH — MERCEDES-MAYBACH, MERCEDES-BENZ S 560 4MATIC, S 650, S 450, S560
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V411000·2018-06-15

    Freightliner Recalls 2018-2019 Cascadia Trucks Due to Brake Caliper Bolt Issue

    Daimler Trucks North America is recalling 2018-2019 Freightliner Cascadia vehicles because brake caliper mounting bolts may not be properly tightened, potentially leading to reduced braking performance.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V409000·2018-06-15

    Thomas Built Buses Recalls Saf-T-Liner EFX School Buses for Brake Defect

    Daimler Trucks North America is recalling 2017-2018 Thomas Built Buses Saf-T-Liner EFX school buses because an incorrectly plumbed check valve may cause sudden parking brake activation and increase crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E040000·2018-06-14

    Dexter Ventline Recalls LP Bottle Straps for Insufficient Crimping

    Dexter Ventline is recalling specific LP bottle straps because insufficient crimping may allow the buckle to detach. This could cause the propane tank to fall from the trailer, creating a road hazard.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V397000·2018-06-14

    General Motors Recalls 2013 Chevrolet Volt for Propulsion Loss Risk

    General Motors is recalling 2013 Chevrolet Volt vehicles because a software update may disable cell balancing, causing a low-voltage condition that could lead to a loss of propulsion and increased crash risk.

    Product
    CHEVROLET — CHEVROLET VOLT
    Category
    Vehicle
    Distribution
    Distributed nationwide