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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17226–17250 of 39601

  • SevereFDA (Devices)·Z-3120-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail 130¿ 11 mm x 180 mm, Item Number: 814511180
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3123-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 11 mm x 300 mm, Item Number: 814511300
    Category
    Medical Device
    Distribution
    42 states
  • SevereNHTSA·18V641000·2018-09-19

    Daimler Trucks Recalls 2019 Freightliner and Western Star Trucks for Tire Defect

    Daimler Trucks is recalling 2019 Freightliner and Western Star trucks because exposed tire sidewall steel cords may cause rapid air loss, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR BUSINESS CLASS M2, 4900, 4700, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V639000·2018-09-17

    Audi Recalls 2017-2018 R8 Vehicles Due to Transmission Fluid Leak Fire Risk

    Volkswagen Group of America is recalling 2017-2018 Audi R8 Spyder and Coupe vehicles because transmission fluid may leak from the gearbox ventilation hose, creating a fire risk if it contacts hot engine parts.

    Product
    AUDI — AUDI R8 SPYDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V642000·2018-09-17

    Heil Recalls 2014-2016 Garbage Trucks Due to Cracking Hydraulic Brackets

    Heil Environmental is recalling 2014-2016 garbage trucks because hydraulic oil tank brackets may crack, causing oil leaks that increase crash risk.

    Product
    HEIL — HEIL SIDE LOADER GARBAGE TRUCK, ROLLOFF BODY/HOIST, FRONT END LOADER GARBAGE, REAR LOADER GARBAGE TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V638000·2018-09-14

    Trail King Recalls 2016-2018 Trailers Due to Cracking Cross Members

    Trail King is recalling 2016-2018 ACS and AACS trailers because aluminum cross members may crack, potentially causing the suspension to loosen and increasing crash risk.

    Product
    TRAIL KING — TRAIL KING AACS, ACS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V636000·2018-09-14

    Alfa Romeo Giulia and Stelvio Recalled for Engine Fire Risk

    Chrysler is recalling 2017-2018 Alfa Romeo Giulia and 2018 Stelvio vehicles because engine misfires may overheat the catalytic converter, potentially causing a fire or engine stall.

    Product
    ALFA ROMEO — ALFA ROMEO STELVIO, GIULIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V621000·2018-09-14

    Mitsubishi Recalls Outlander Models Due to Safety System Software Defect

    Mitsubishi is recalling 2017-2018 Outlander, Outlander Sport, Eclipse Cross, and Outlander PHEV vehicles because incorrect software may prevent safety systems like automatic emergency braking from functioning.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER, OUTLANDER SPORT, ECLIPSE CROSS, OUTLANDER PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V635000·2018-09-14

    Alfa Romeo Stelvio Recall: Engine Cooling Hose Defect

    Chrysler is recalling 2018-2019 Alfa Romeo Stelvio Quadrifoglio vehicles because an engine cooling hose may leak coolant, causing overheating and stalling.

    Product
    ALFA ROMEO — ALFA ROMEO STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V633000·2018-09-14

    Cruiser RV Recalls 2019 Travel Trailers Due to Axle Bearing Defect

    Cruiser RV is recalling 2019 travel trailers because missing inner bearing races may cause hub failure and increase crash risk.

    Product
    CRUISER RV — CRUISER RV MPG, EMBRACE, FUN FINDER EXTREME LITE, SHADOW CRUISER ULTRA LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V630000·2018-09-13

    Honda Recalls 2018 CRF250L Motorcycles Due to Wiring Harness Defect

    Honda is recalling 2018 CRF250L motorcycles because an improperly installed wiring harness may damage safety components like lights and the horn, increasing crash risk.

    Product
    HONDA — HONDA CRF250L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V628000·2018-09-13

    Forest River Recalls 2019 East to West Travel Trailers Due to Axle Issue

    Forest River is recalling 2019 East to West travel trailers because incorrect axle shackles may allow tires to contact the wheel well, risking tire failure and loss of control.

    Product
    FOREST RIVER — FOREST RIVER EAST TO WEST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V624000·2018-09-13

    Forest River Recalls 2019 Travel Trailers Due to Axle Bearing Defect

    Forest River is recalling 2019 travel trailers because missing inner bearing races may cause hub overheating or separation, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN XLR, VIBE, SIERRA, SHASTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V617000·2018-09-12

    Altec Recalls 2018 Cranes, Derricks, and Aerial Devices Due to Fastener Defect

    Altec Industries is recalling 2018 cranes, digger derricks, and aerial devices because overtightened fasteners may break, potentially causing the platform to separate from the vehicle.

    Product
    ALTEC — ALTEC DIGGER DERRICK, CRANE, AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1173-2018·2018-09-12

    AvKARE Valsartan and Hydrochlorothiazide Tablets Recalled for Carcinogen Impurity

    AvKARE is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    AvKARE Valsartan and Hydrochlorothiazide 80 mg/12.5 mg tablets, 90-count bottle, Rx Only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478, NDC 42291-884-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1176-2018·2018-09-12

    AvKARE Valsartan and Hydrochlorothiazide Tablets Recalled for Carcinogen Impurity

    AvKARE is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    AvKARE Valsartan and Hydrochlorothiazide 320 mg/12.5 mg tablets, 90-count bottle, Rx Only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478, NDC 42291-886-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2990-2018·2018-09-12

    GE Vivid E7 Ultrasound System Recalled for Power Cord Shock Risk

    GE Medical Systems is recalling Vivid E7 ultrasound systems because the power cord may break and expose electrical conductors, creating a risk of electric shock.

    Product
    GE Vivid E7 ultrasound system Product Usage: Vivid E7 is a general-purpose ultrasound system, specialized for use in cardiac imaging. It is intended for use by, or under the direction of a qualified physician for ultrasound imaging and analysis of Fetal/Obstetrics; Abdominal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1174-2018·2018-09-12

    AvKARE Valsartan and Hydrochlorothiazide Tablets Recalled for Carcinogen Impurity

    AvKARE is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    AvKARE Valsartan and Hydrochlorothiazide 160 mg/12.5 mg tablets, 90-count bottle, Rx Only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478, NDC 42291-885-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1177-2018·2018-09-12

    AvKARE Valsartan and Hydrochlorothiazide Tablets Recalled for Carcinogen Impurity

    AvKARE is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    AvKARE Valsartan and Hydrochlorothiazide 320 mg/25 mg tablets 90-count bottle, Rx Only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478, NDC 42291-888-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1931-2018·2018-09-12

    El Guapo Jamaica Hibiscus Flowers Recalled for Undeclared Allergen

    Mojave Foods Corp. is recalling El Guapo Jamaica Hibiscus Flowers in various pouch sizes due to an undeclared allergen.

    Product
    El Guapo Jamaica Hibiscus Flowers in flexible pouches , 1 oz., 2 oz., 8 oz., 16 oz., and 10 lb. box .
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Devices)·Z-2980-2018·2018-09-12

    Medline Recalls LASER CDS Surgical Packs with Non-Sterile Applicators

    Medline Industries is recalling 144 LASER CDS surgical kits because specific ChloraPrep applicators were not sterilized. The non-sterile components were inadvertently released to California and New Mexico.

    Product
    LASER CDS
    Category
    Medical Device
    Distribution
    2 states