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.

Filters

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

11276–11300 of 36636

  • SevereFDA (Devices)·Z-1932-2020·2020-05-20

    Philips Zenition 50 Medical Device Recalled for Electrical Contact Failure

    Philips is recalling 25 Zenition 50 devices because strain relief loss can cause electrical contacts to break, potentially exposing live parts or losing the video signal.

    Product
    Philips Zenition 50, System code 718096 - Product Usage: The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical procedures on all patients, except neonates (birth to one month), within the limits of the device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V293000·2020-05-20

    Vac-Tron Vacuum Excavator Trailers Recalled for Rear Impact Protection Defect

    Vac-Tron is recalling 2016-2020 vacuum excavator trailers because the rear extends too far, failing federal safety standards and increasing crash risks.

    Product
    VAC-TRON — VAC-TRON CS 1270 GT, CS 870 GT, CS 873 GT, CV 1273 GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1960-2020·2020-05-20

    Intuitive Surgical Recalls da Vinci Xi Systems Due to Arm Faults

    Intuitive Surgical is recalling 74 da Vinci Xi Surgical Systems because a manufacturing variation can cause arm faults and loss of functionality during surgery.

    Product
    da Vinci Xi Surgical System
    Category
    Medical Device
    Distribution
    13 states
  • SevereFDA (Devices)·Z-1945-2020·2020-05-20

    Beckman Coulter iQ200 Urine Analyzer Recalled for Electrical Short Risk

    Beckman Coulter is recalling iQ200 Series Urine Microscopy Analyzers due to a defect in the SATA power adapter cable that poses a risk of electrical short, charring, smoke, or flames.

    Product
    iQ200 Series Urine Microscopy Analyzer- All part numbers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1944-2020·2020-05-20

    Beckman Coulter iChem VELOCITY Urine Chemistry System Recalled for Fire Risk

    Beckman Coulter is recalling iChem VELOCITY Urine Chemistry Systems due to a defect in the SATA power adapter cable that poses a risk of electrical short, smoke, or flames.

    Product
    iChem¿VELOCITY Urine Chemistry System-
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V284000·2020-05-20

    REV Recalls 2018-2020 Type 1 Ambulances for Rear Brake Line Wear

    REV is recalling 2018-2020 Type 1 ambulances because a rear brake line may wear, causing brake failure and increasing crash risk.

    Product
    FRONTLINE — FRONTLINE, ROAD RESCUE, WHEELED COACH TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V291000·2020-05-20

    Horton Emergency Vehicles Recalled for Rear Brake Line Wear Risk

    Halcore is recalling 2018-2020 Horton ambulances because a rear brake line may wear from contact with suspension parts, risking brake loss.

    Product
    HORTON — HORTON TYPE III, TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1957-2020·2020-05-20

    Siemens Cios Alpha Mobile X-Ray System Recalled for Electrical Shock Risk

    Siemens is recalling four Cios Alpha mobile X-ray systems because unplugging the main cable during a clinical session can expose users to unsafe electrical voltage.

    Product
    Siemens Cios Alpha VA20-mobile X-Ray system Material # 10308191 The Cios Alpha and Cios Spin are a mobile X-Ray system designed to provide X-ray imaging of the anatomical structures of patient during clinical applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1933-2020·2020-05-20

    Philips Zenition 70 Trolley Cable Recall for Electrical Contact Failure

    Philips is recalling 25 Zenition 70 systems because strain relief loss on the trolley cable can break electrical contacts, exposing live parts.

    Product
    Philips Zenition 70, System code 718133 - Product Usage: The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical procedures on all patients, except neonates (birth to one month), within the limits of the device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1991-2020·2020-05-20

    FDA Recalls Dover Foley Catheters Due to Temperature Sensor Inaccuracy

    The FDA is recalling specific lots of Dover Foley catheters because their temperature sensors may not measure accurately. This could lead to incorrect patient diagnoses.

    Product
    Dover 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley Tray 400mL, Premium, Urine Meter, 16 Fr/Ch (5.3 mm), 5 mL Catheter Pre-connected to 2000 mL Drainage Bag with Luer-Lock Sampling, Temperature Sensor and Adhesive Catheter Securement, Sterile, Product Code…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1269-2020·2020-05-20

    MasterPharm Recalls Finasteride Plus Capsules Due to Minoxidil Contamination

    MasterPharm LLC is recalling Finasteride Plus 1.25 mg capsules because they were found to contain minoxidil. The recall covers 7,260 capsules distributed nationwide.

    Product
    Finasteride Plus 1.25 mg Capsule, a) 30-count bottle, b) 90-count bottle, Compounded Product Not for Resale, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0945-2020·2020-05-20

    Whole Foods Market Queso Sauce Recalled for Undeclared Cashews

    Whole Foods Market is recalling Queso Sauce sold in Arizona due to a potential undeclared cashew allergen.

    Product
    Whole Foods Market Queso Sauce PLU code printed on the product scale labels beginning with 74135 sold in clear plastic deli-style containers of various weights.
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·20V283000·2020-05-20

    BMW and MINI Recall Vehicles Due to Rollover Sensor Defect

    BMW is recalling certain 2020-2021 vehicles because a rollover sensor defect may prevent air bags and seat belt pretensioners from deploying in a crash.

    Product
    MINI — MINI, BMW COOPER S CLUBMAN, X1, X2, COOPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V282000·2020-05-19

    Altec Recalls Aerial Devices and Digger Derricks Due to Bolt Failure Risk

    Altec is recalling 2018-2020 aerial devices and digger derricks because bolts securing the pedestal to the turntable may fail, increasing the risk of injury or death.

    Product
    ALTEC — ALTEC AERIAL DEVICE, DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V279000·2020-05-18

    Mitsubishi Recalls Lancer and Outlander Models for Corroded Front Cross Members

    Mitsubishi is recalling specific Lancer, Outlander, and Outlander Sport vehicles because front cross members may corrode and detach, increasing crash risk.

    Product
    MITSUBISHI — MITSUBISHI LANCER, OUTLANDER, OUTLANDER SPORT, LANCER SPORTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V281000·2020-05-18

    Western Star 4700 and 5700 trucks recalled for ground harness wiring defect

    DTNA is recalling certain 2019-2021 Western Star 4700 and 5700 trucks. An undersized wire in the ground harness may cause a melted connector, leading to engine stall and increasing crash risk.

    Product
    WESTERN STAR — WESTERN STAR 4700, 5700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20122·2020-05-14

    Garia Recalls Electric Golf and Courtesy Vehicles Due to Fire Hazard

    Garia is recalling about 1,000 battery-powered golf and courtesy vehicles because a fuse can overheat and melt while charging, posing a fire hazard.

    Product
    Garia Golf & Courtesy battery-powered electric vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1847-2020·2020-05-13

    Applied Medical Recalls Bard Embolectomy Catheters Due to Tip Separation

    Applied Medical Resources Corp is recalling Bard Embolectomy Catheters because the tips may separate during use, posing a risk of dislodgement in patients.

    Product
    Bard Embolectomy Catheter & 1 ml SYRINGE, REF numbers/UDI: CE0340DR/(01)H699CE0340DR10R; CE0380DR/(01)H699CE0380DR10V; CE0440DR/(01)H699CE0440DR10S; CE0480DR/(01)H699CE0480DR10W; CE0540DR/(01)H699CE0540DR10T; CE0580DR/(01)H699CE0580DR10X…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1842-2020·2020-05-13

    Philips Recalls Transesophageal Ultrasound Transducers Due to Temperature Measurement Defect

    Philips Ultrasound Inc is recalling S7-3t transesophageal transducers because a programming error prevents the system from measuring tip temperature, which may stop auto-cooling and cause patient injury.

    Product
    Transducer S7-3t UDI (01)00884838067530 REF 989605439232 Used as accessory with: iE33, HD11 Ultrasound Systems - Product Usage: Diagnostic ultrasound imaging or fluid flow analysis of the human body - particularly transesophageal echocardiography (TEE) studies
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1900-2020·2020-05-13

    Howmedica Recalls Cortoss Bone Augmentation Material Due to Temperature Violations

    Howmedica Osteonics Corp. is recalling 115 units of Cortoss Bone Augmentation Material because shipments were transported outside required refrigerated temperature conditions.

    Product
    Cortoss Bone Augmentation Material, Catalog Nos. 2101-0005 and 2101-0010
    Category
    Medical Device
    Distribution
    15 states
  • SevereFDA (Food)·F-0938-2020·2020-05-13

    Medifast Recalls Optavia Oatmeal Pouches Due to Undeclared Milk

    Medifast is recalling Optavia Old Fashioned Maple & Brown Sugar Oatmeal pouches because they contain undeclared milk.

    Product
    Optavia, Old Fashioned Maple & Brown Sugar Oatmeal . 1.13 oz./ 32 g pouch, Multi-layer Kraft paper/aluminum pouches, Seven pouches per carton
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1791-2020·2020-05-13

    Argon Medical Devices Recalls 0.035 Inch Guidewires Due to Tissue Perforation

    Argon Medical Devices is recalling specific 0.035-inch guidewires because the stiffness of the soft end caused tissue perforation. The affected units were distributed to several countries outside the United States.

    Product
    0.035"(.89mm)x80 cm guidewire. Model 114135080. Soft Tip 3.5cm. REF/UDI: 114135080/(01)208863333008067. RxOnly STERILE EO
    Category
    Medical Device
    Distribution
    0 states