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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16776–16800 of 39599

  • SevereNHTSA·18V819000·2018-11-20

    Heartland Recalls 2019 Trailers Due to Bearing Grease Defect

    Heartland is recalling 2019 Pioneer and Prowler trailers because inner hub bearings may overheat and fail, increasing crash risk.

    Product
    HEARTLAND — HEARTLAND PIONEER, PROWLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V821000·2018-11-20

    Navistar Recalls 2019-2020 IC Bus CE School Buses for Brake Line Defect

    Navistar is recalling 187 IC Bus CE school buses from 2019-2020 because an improperly routed brake air line may kink, causing the vehicle to pull right or disabling anti-lock brakes.

    Product
    IC BUS — IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19036·2018-11-20

    Seabreeze Recalls Smart Thermaflo Bathroom Heater Fans Due to Fire Hazard

    Seabreeze International is recalling Smart Thermaflo Bathroom Heater Fans because the safety cutoff can fail, allowing the unit to overheat and catch fire.

    Product
    Smart Thermaflo Bathroom Heater Fans with nightlight
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V818000·2018-11-19

    Audi Recalls Q5 and Q7 Models for Fuel Pump Flange Repair

    Volkswagen Group of America is recalling 2007-2012 Audi Q7 and 2009-2012 Audi Q5 vehicles to replace fuel pump flanges and install butyl tape to prevent fuel leaks and fire risk.

    Product
    AUDI — AUDI Q5, Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·114-2018·2018-11-17

    Swift Beef Company Recalls Ground Beef Due to E. coli O157:H7

    Swift Beef Company is recalling approximately 99,260 pounds of raw ground beef products that may be contaminated with E. coli O157:H7. The products were distributed in California, Nevada, Oregon, Utah, and Washington.

    Product
    Swift Beef Company — Swift Beef Company Recalls Ground Beef Products due to Possible E. coli O157:H7 Contamination
    Category
    Food
    Distribution
    5 states
  • CriticalUSDA FSIS·113-2018·2018-11-16

    Majestic Meat Company Recalls Ground Beef for E. coli O157:H7

    Majestic Meat Company is recalling approximately 532 pounds of ground beef products in Utah due to possible E. coli O157:H7 contamination.

    Product
    Corfini Meat and Seafood — Majestic Meat Company Recalls Ground Beef Products due to Possible E. coli O157:H7 Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·18V815000·2018-11-16

    Autocar Recalls 2019 Xpeditor Vehicles Due to Steering Bracket Defect

    Autocar is recalling 761 2019 Xpeditor vehicles because the power steering assist cylinder bracket may not be properly secured, potentially causing a loss of steering ability.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V813000·2018-11-16

    ARBOC Transit Bus Recall for Foldaway Seat Locking Defect

    ARBOC is recalling 2015-2018 Spirit of Freedom, Mobility, and Independence buses because foldaway seat cushions may not stay locked during a crash.

    Product
    ARBOC — ARBOC, ARBOC SPECIALTY VEHICLES SPIRIT OF INDEPENDENCE, SPIRIT OF MOBILITY, SPIRIT OF FREEDOM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19717·2018-11-15

    RH Recalls Metal-Wrapped Coffee Tables Due to Lead Exposure Risk

    Restoration Hardware is recalling specific metal-wrapped coffee tables because the metal tops may contain lead, posing a health risk to children.

    Product
    Metal-wrapped coffee tables
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V810000·2018-11-15

    Mack Trucks Recalls 2019 Models Due to Tire Air Loss Risk

    Mack is recalling 818 2019 LR, Granite, and TerraPro trucks because specific Bridgestone tires may lose air rapidly, increasing crash risk.

    Product
    MACK — MACK LR, GRANITE (GR), TE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·112-2018·2018-11-15

    Jennie-O Recalls Raw Ground Turkey Due to Salmonella Reading Contamination

    Jennie-O is recalling raw ground turkey products produced in September 2018 due to possible Salmonella Reading contamination linked to a multi-state outbreak.

    Product
    Jennie-O Turkey Store Sales, LLC Recalls Raw Ground Turkey Products due to Possible Salmonella Reading Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0269-2019·2018-11-14

    OriGen Reinforced Dual Lumen Cannula Recalled for Potential Tube Separation

    OriGen Biomedical is recalling 134 units of the VV19F Reinforced Dual Lumen Cannula because the extension tube may separate from the hub, posing a risk of blood loss.

    Product
    REF VV19F Reinforced Dual Lumen Cannula, 19Fr., Sterile EO, DISPOSABLE: DO NOT RE-USE CE 0473 Product Usage: The OriGen RDLC catheter is indicated for use as a single cannula for both venous drainage and arterial re-infusion of blood in the internal jugular vein during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0251-2019·2018-11-14

    Native Remedies VertiFree Oral Spray Recalled for Microbial Contamination

    Silver Star Brands is recalling Native Remedies VertiFree Oral Spray due to microbial contamination. Consumers should stop using the product and return it to the point of purchase.

    Product
    Native Remedies VertiFree Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906. NDC 68703-253-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0254-2019·2018-11-14

    Silver Star Brands Recalls Native Remedies EyeClear Pro Oral Spray

    Silver Star Brands is recalling Native Remedies EyeClear Pro Oral Spray due to microbial contamination. Consumers should stop using the product and return it to the retailer.

    Product
    Native Remedies EyeClear Pro Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906. NDC 68703-151-59
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0253-2019·2018-11-14

    Silver Star Brands Recalls Native Remedies VaricoGo Oral Spray Due to Microbial Contamination

    Silver Star Brands is recalling 53 bottles of Native Remedies VaricoGo Oral Spray due to microbial contamination. The product was distributed nationwide in the United States.

    Product
    Native Remedies VaricoGo Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906. NDC 68703-105-59
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·111-2018·2018-11-14

    Ron's Home Style Foods Recalls Chicken Salad Products Due to Listeria Risk

    Ron's Home Style Foods is recalling approximately 6,912 pounds of ready-to-eat chicken salad products in Texas due to possible Listeria monocytogenes contamination.

    Product
    Ron's Home Style Foods — Ron's Home Style Foods Recalls Ready to Eat Chicken Salad Products due to Possible Listeria Contamination
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0432-2019·2018-11-14

    ARO Pistachios Recalls Pistachios Due to Salmonella Test Results

    ARO Pistachios, Inc. is recalling one lot of inshell pistachios after a customer test detected Salmonella.

    Product
    Inshell R/S 21/25 US-Select Pistachios NET WT. 25 lbs. 11.34 kg Product of the USA ARO Pistachio Inc. 19570 Avenue 88, Terra Bella, Ca 93270
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0252-2019·2018-11-14

    Silver Star Brands Recalls Native Remedies HypoSlim Oral Spray Due to Microbial Contamination

    Silver Star Brands is recalling 95 bottles of Native Remedies HypoSlim Oral Spray due to microbial contamination. The product was distributed nationwide in the US.

    Product
    Native Remedies HypoSlim Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906. NDC 68703-275-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0233-2019·2018-11-14

    Qualgen Recalls Testosterone Pellets Due to Sterility Assurance Concerns

    Qualgen, LLC is recalling specific lots of Testosterone 200mg pellets nationwide due to a lack of assurance of sterility.

    Product
    Testosterone 200mg pellet, 1 count (NDC 69761-120-01), 6 count (NDC 69761-120-06), 12 count (NDC 69761-120-12), and 30 count (NDC 69761-120-30) vials, Rx Only Qualgen, LLC, Edmond, OK 73013
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0225-2019·2018-11-14

    Qualgen Recalls Estradiol Pellets Due to Lack of Sterility Assurance

    Qualgen, LLC is recalling Estradiol 10mg pellets nationwide due to a lack of assurance of sterility. The affected lots have specific expiration dates.

    Product
    Estradiol 10mg pellet, 1 count (NDC 69761-010-01), 6 count (NDC 69761-010-06), 12 count (NDC 69761-010-12), and 30 count (NDC 69761-010-30) vials, Rx Only, Qualgen, LLC, Edmond, OK 73013
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0237-2019·2018-11-14

    Qualgen Recalls Testosterone Pellets Due to Sterility Concerns

    Qualgen, LLC is recalling specific lots of Testosterone 87.5mg pellets nationwide due to a lack of assurance of sterility.

    Product
    Testosterone 87.5mg pellet, 1 count (NDC 69761-187-01), 6 count (NDC 69761-187-06), 12 count (NDC 69761-187-12), and 30 count (NDC 69761-187-30) vials, Rx Only Qualgen, LLC, Edmond, OK 73013
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0360-2019·2018-11-14

    Roche CoaguChek XS Prothrombin Time Test Strips Recalled for High INR Results

    Roche Diagnostics is recalling CoaguChek XS Prothrombin Time test strips nationwide because they may produce abnormally high INR results.

    Product
    CoaguChek¿ XS System Prothrombin time test: CoaguChek XS PT Test 2X24 Strips, Catalog Number: 04625315160; CoaguChek XS PT Test 6 Strips, Catalog Number: 04625374160; CoaguChek XS PT Test 24 Tests, Catalog Number: 07797826160;
    Category
    Medical Device
    Distribution
    Distributed nationwide