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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26326–26350 of 90150

  • HighFDA (Devices)·Z-0781-2022·2022-03-23

    Boston Scientific RX Cholangiogram Kit Recall Due to Sterile Barrier Breach

    Boston Scientific is recalling RX Cholangiogram Kits because the sterile barrier has been breached, compromising the sterility of the devices. The affected kits were distributed worldwide.

    Product
    RX CHOLANGIOGRAM KIT - SINGLE Material Number: M00575240 M00575240 M00575280 M00575320 M00575360 M00575380 M00575400 M00575440 M00575480
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0766-2022·2022-03-23

    Boston Scientific recalls 68 medical devices with sterility breach

    Boston Scientific is recalling 68 JAGTOME REVOLUTION RX medical devices due to sterile barrier breach. The devices were distributed worldwide including throughout the US.

    Product
    JAGTOME REVOLUTION RX 39-20-450-025 Material Number: M00584250
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0762-2022·2022-03-23

    HYDRATOME RX surgical device recalled due to sterile barrier breach

    Boston Scientific recalls 251 HYDRATOME RX 44-30MM/450CM units worldwide due to sterile barrier breach that compromises device sterility.

    Product
    HYDRATOME RX 44-30MM/450CM Material Number: M00583070
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0790-2022·2022-03-23

    FDA Recalls Safe-T PLUS Pediatric Lumbar Puncture Tray Due to Manometer Failure

    Bard Peripheral Vascular Inc is recalling 20,400 Safe-T PLUS pediatric lumbar puncture trays due to manometer leaking and mating failures. The devices were distributed nationwide and internationally to healthcare facilities.

    Product
    Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray, 22 g x 1.5" Spinal Needle with Manometer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0886-2022·2022-03-23

    Stutzman Farms Organic All Purpose Flour Recalled for Undeclared Wheat Allergen

    Stutzman Farms is recalling its Organic All Purpose Flour sold in bulk due to undeclared wheat allergen. The flour was distributed across seven states and may affect individuals with wheat allergies.

    Product
    Stutzman Farms Organic All Purpose Flour sold in bulk
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0771-2022·2022-03-23

    Medical Device Recall: Boston Scientific JAGTOME RX Sterile Barrier Breach

    Boston Scientific is recalling 98 units of the JAGTOME RX 39-30-260-025 medical device due to compromised sterile barrier that affects device sterility. Units were distributed worldwide.

    Product
    JAGTOME RX 39-30-260-025 Material Number: M00573100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0859-2022·2022-03-23

    Salted Dried Plums Recalled for High Lead Levels

    Vbest Inc is recalling salted dried plums (saladitos) distributed in California and Washington due to high lead levels detected by the California Department of Public Health. Consumers should not consume the affected product.

    Product
    Salted Dried Plums, 500kgcartons, 20kgs plastic bag/carton
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0778-2022·2022-03-23

    Boston Scientific JAGTOME RX Recalled for Sterile Barrier Breach

    Boston Scientific is recalling 96 units of JAGTOME RX medical devices due to a sterile barrier breach that compromises device sterility. Patients should contact their physician if they received this device.

    Product
    JAGTOME RX 49-30-260-035 Material Number: M00573020
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0891-2022·2022-03-23

    Broccoli Cheddar Pasta Salad Recalled Due to Hard Plastic Contamination

    Walmart's Freshness Guaranteed Broccoli Cheddar Pasta Salad is recalled due to hard plastic pieces found during manufacturing. The contamination came from ice purchased from a supplier and affects products with use-by dates of March 14–22, 2022.

    Product
    Freshness Guaranteed BROCCOLI CHEDDAR PASTA SALAD WM 6/14 OZ (397 g) UPC: 0 78742 37256 3 Distributed by Walmart Inc., Bentonville, AR 72716
    Category
    Food
    Distribution
    20 states
  • HighFDA (Devices)·Z-0776-2022·2022-03-23

    Medical Device Sterile Barrier Breach: JAGTOME RX Recall

    Boston Scientific is recalling JAGTOME RX medical devices because the sterile barrier may be compromised, which could allow contamination. The recall affects 163 units distributed worldwide.

    Product
    JAGTOME RX 44-30-450-035 Material Number: M00573070
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V172000·2022-03-22

    Marion Body Works Recalls 2018 International SR525 Emergency Vehicle

    Marion Body Works is recalling one 2018 International SR525 emergency vehicle because the engine may overcome the parking brake, increasing crash risk.

    Product
    MARION BODY WORKS — MARION BODY WORKS INTERNATIONAL SR525
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V173000·2022-03-22

    Hi-Tech E.V.S. Recalls Spartan Emergency Vehicles for Display Defect

    Hi-Tech E.V.S. is recalling 2020 Spartan MetroStar and 2021 Spartan Gladiator emergency vehicles because LCD displays may lock up, potentially delaying emergency efforts.

    Product
    HI-TECH E.V.S. — HI-TECH E.V.S. SPARTAN METROSTAR, SPARTAN GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V170000·2022-03-21

    2022 Heartland Travel Trailers Recalled for Electrical Fire Risk

    Heartland is recalling certain 2022 Trail Runner, Prowler, and Lithium travel trailers with defective power inlet bolts that may loosen, creating an electrical fire hazard. Dealers will inspect and replace the inlet free of charge.

    Product
    HEARTLAND — HEARTLAND PROWLER, LITHIUM, TRAIL RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E023000·2022-03-19

    ZH Brothers Recalls Epicord 50-amp Shore Power Inlets Due to Fire Risk

    ZH Brothers is recalling Epicord 50-amp Shore Power Inlets because loose wiring connections may cause electrical arcs or shorts, increasing the risk of fire.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V168000·2022-03-18

    Mercedes-Benz Recalls Vehicles for Software Configuration Errors

    Mercedes-Benz is recalling specific 2007-2014 models because incorrect software updates may cause loss of drive power or control functions, increasing crash risk.

    Product
    MERCEDES BENZ — MERCEDES BENZ, MERCEDES-BENZ C300, C350, E350, G550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E021000·2022-03-18

    Dometic Recalls 2-Burner Cooktops Due to Gas Leak Risk

    Dometic is recalling specific 2-burner cooktops because damaged burner control valves may cause a gas leak, increasing the risk of fire.

    Product
    EQUIPMENT:APPLIANCE:OVEN/STOVE/COOKTOP recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V167000·2022-03-18

    Mercedes-Benz Recalls S-Class and EQS Models for Turn Signal Software Error

    Mercedes-Benz is recalling 2021 S 500/S 580 and 2022 EQS 450/580 vehicles because a software error may disable rear turn signals, hazard lights, and reverse lights.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ S 500, EQS 580, EQS 450, S 580
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V169000·2022-03-18

    Tesla Recalls Model 3, S, and X for Rearview Camera Delay

    Tesla is recalling certain Model 3, S, and X vehicles because the rearview camera image may not display immediately when reversing, increasing crash risk.

    Product
    TESLA — TESLA MODEL 3, MODEL S, MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·22101·2022-03-17

    HD Premier Recalls DigitDots Magnetic Balls Due to Ingestion Hazard

    HD Premier is recalling DigitDots 3mm and 5mm magnetic balls because swallowed magnets can lodge in the digestive system, causing perforation, blockage, infection, and potentially death. Four children have required surgery to remove ingested DigitDots.

    Product
    DigitDots 3mm and 5mm Magnetic Balls
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·22734·2022-03-17

    ToolGuards Portable Water Immersion Heaters Recalled for Shock and Fire Hazards

    FXswede AB is recalling about 5,000 ToolGuards Portable Water Immersion Heaters sold on Amazon.com because the units can overheat, melt, or catch fire, creating electrocution and fire hazards. The firm has received 19 reports of overheating or fires and 2 reports of consumer shock.

    Product
    ToolGuards Portable Water Immersion Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V166000·2022-03-17

    Newmar motorhomes recalled for loose steering column bolt

    Newmar is recalling 1,277 of its 2021 and 2022 motorhomes because the steering column bolt may not be properly tightened, potentially causing loss of steering control. Owners should contact dealers for free inspection and tightening.

    Product
    NEWMAR — NEWMAR NEW AIRE, DUTCH STAR, LONDON AIRE, KOUNTRY STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V164000·2022-03-17

    International LT vehicles recalled for battery cable fire risk

    Navistar is recalling 2018-2023 International LT vehicles with 1500W Purkeys inverter systems. The positive battery cable may be incorrectly routed, causing it to chafe and become damaged, which increases the risk of electrical fire.

    Product
    INTERNATIONAL — INTERNATIONAL LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V165000·2022-03-17

    GM Recalls 2014-2015 Chevrolet Equinox and GMC Terrain for Wiper Defect

    General Motors is recalling 2014-2015 Chevrolet Equinox and GMC Terrain vehicles because corroded ball joints may cause windshield wipers to fail, reducing visibility.

    Product
    GMC — GMC, CHEVROLET TERRAIN, EQUINOX
    Category
    Vehicle
    Distribution
    Distributed nationwide