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 deaths or serious injuries are reported, 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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4426–4450 of 36541

  • SevereNHTSA·24V097000·2024-02-09

    2021-2022 Ford E-350 and E-450 Power Steering Fluid Loss Recall

    Ford is recalling certain 2021-2022 E-350 and E-450 vehicles due to a defective power steering connection that may cause loss of power steering fluid and brake assist.

    Product
    FORD — FORD E-350, E-450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V101000·2024-02-09

    Foretravel Recalls 2023 Realm Vehicles Due to Steering Gear Defect

    Foretravel is recalling 2023 Realm and Realm Presidential vehicles because foreign material in the steering gear may cause a loss of power steering assist, increasing crash risk.

    Product
    FORETRAVEL — FORETRAVEL REALM, REALM PRESIDENTIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E010000·2024-02-09

    R.H. Sheppard Recalls Steering Gears Due to Fracture Risk

    R.H. Sheppard is recalling steering gears where the sector shaft may have been improperly heat-treated, potentially causing cracks or fractures that lead to loss of steering control.

    Product
    STEERING:GEAR BOX:SHAFT SECTOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24109·2024-02-08

    Vornado Handheld Garment Steamers Recalled for Burn Hazard

    Vornado, Steamfast, and Sharper Image-branded handheld garment steamers can expel hot water from the steam nozzle, posing a serious burn hazard. About 2 million units sold nationwide are affected.

    Product
    Steamfast, Vornado and Sharper Image-branded handheld garment steamers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24113·2024-02-08

    Husqvarna Gas-Powered Grass Trimmers Recalled for Fire Hazard

    Husqvarna is recalling about 403,000 gas-powered grass trimmers due to incorrect wiring in the ignition module that can cause electrical sparks or arcing, creating a fire hazard. The firm has received 12 reports of fires, including one burn injury.

    Product
    Gas-powered Grass Trimmers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V093000·2024-02-08

    2024 FCCC MT45 and Freightliner Cascadia steering gear recall

    Daimler Trucks North America is recalling certain 2024 FCCC MT45 and Freightliner Cascadia vehicles due to steering gear assembly defects that may result in loss of steering control. Contact dealers or call 1-800-745-8000 for free replacement of the affected component.

    Product
    FREIGHTLINER — FREIGHTLINER, FCCC CASCADIA, MT45G, MT45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V084000·2024-02-08

    Western Star 49X Suspension Hanger Defect May Affect Steering Control

    Daimler Trucks North America is recalling 2022-2024 Western Star 49X vehicles with suspension hangers that may fail due to missing welds, potentially impairing steering and directional control.

    Product
    WESTERN STAR — WESTERN STAR 49X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V088000·2024-02-08

    2024 International Trucks Steering Defect May Cause Loss of Control

    Navistar recalls 2024-2025 International trucks and 2024 IC Bus commercial buses due to steering gear assemblies that may be incorrectly assembled, potentially causing loss of steering control.

    Product
    INTERNATIONAL — INTERNATIONAL, IC BUS RH, MV, HV, HX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V092000·2024-02-08

    Vicinity Recalls 2022 Vi35 Buses Due to CNG Tank Clearance Issue

    Vicinity is recalling 2022 Vi35 transit buses because inadequate clearance may damage CNG tanks, increasing the risk of natural gas leaks and fire.

    Product
    VICINITY — VICINITY VI35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V089000·2024-02-08

    Navistar Recalls 2024 IC Bus CE School Buses for Steering Defect

    Navistar is recalling 2024 IC Bus CE school buses because steering gear assemblies may have fewer recirculating balls than required, risking loss of steering control.

    Product
    IC BUS — IC BUS CE SBUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0282-2024·2024-02-07

    FDA Recalls Vancomycin IV Bags Due to Dosing System Malfunction

    Denver Solutions is recalling 7,548 IV bags of vancomycin due to a manufacturing system malfunction that can deliver double doses. The product was distributed nationwide.

    Product
    VANCOmycin HCl PF 1.5g added to 0.9% Sodium Chloride 250 mL IV bag, Item F3208, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-029-68.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0323-2024·2024-02-07

    FDA Recalls Zenzedi Dextroamphetamine Sulfate Due to Label Mix-up

    The FDA has recalled Zenzedi (Dextroamphetamine Sulfate) 30 mg tablets due to a labeling error. The recall affects 4,662 bottles distributed nationwide.

    Product
    ZENZEDI — ZENZEDI (DEXTROAMPHETAMINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0277-2024·2024-02-07

    Fentanyl Citrate IV Bags Recalled Due to Double-Dose Filling System Malfunction

    Denver Solutions recalled 8,976 IV bags of fentanyl citrate nationwide due to a malfunction in the semi-automated filling system that could deliver double the intended dose.

    Product
    FentaNYL citrate PF, 1000 mcg per 100 mL 0.9% Sodium Chloride (10 mcg per mL), Item F3355, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-072-41.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0279-2024·2024-02-07

    Phenylephrine IV Bags Recalled for Double-Dose Filling System Malfunction

    Denver Solutions is recalling 29,016 Phenylephrine HCl IV bags distributed nationwide. A filling system malfunction can result in some bags receiving double doses of this potent injectable drug.

    Product
    PHENYLephrine HCl 20 mg per 250 mL 0.9% Sodium Chloride (80 mcg per mL), Item F3360, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-148-94.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0776-2024·2024-02-07

    Medical Device Compressor Kits Recalled for Elevated Formaldehyde Levels

    GE HealthCare is recalling EvAir compressor kits for CARESCAPE and Engström ventilators due to elevated formaldehyde levels found in preliminary testing. The recall affects 1,294 units distributed worldwide.

    Product
    EvAir CPRSR Kit Upgrade: a) DISS/CEE 7/7 230V 50/60 HZ, Model Number M1230849; b) DISS/NEMA 5-15 115V 60 HZ, Model Number M1230847; c) NIST/BS 1363 230V 50/60 HZ, Model Number M1230849; d) NIST/BS 546 230V 50/60 HZ, Model Number M1230849; e) NIST/CEE 7/7 230V 50/60 HZ,
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Food)·F-0807-2024·2024-02-07

    Fat Choy Kee Dried Longan Recalled for Undeclared Sulfites

    Fat Choy Kee Dried Longan produced by HY SUCCESS INC. is being recalled because it contains undeclared sulfites. Sulfites are a known allergen that poses health risks to sensitive individuals.

    Product
    Fat Choy Kee Dried Longan
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-0864-2024·2024-02-07

    Smiths Medical Medfusion 4000 Syringe Pump Software Defects Recall

    The FDA is recalling Smiths Medical Medfusion Model 4000 syringe pumps due to software defects affecting medication delivery, alarms, and display accuracy. Users should install the latest software version to correct these issues.

    Product
    smiths medical Medfusion Model 4000 syringe pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0939-2024·2024-02-07

    EZDilate Wire Guided Balloon Recalled for Device Malfunction Issues

    Olympus recalls EZDilate Wire Guided Balloon devices used for endoscopic dilation due to reported bursting, leaking, and retrieval failures affecting 1,639 units nationwide.

    Product
    EZDilate Wire Guided Balloon 6-7-8. indicated for endoscopic dilation of strictures in the alimentary tract in adults and adolescents (>12 years) Model: BD-410X-0855
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0278-2024·2024-02-07

    FentaNYL Citrate IV Bags Recalled Due to Double-Dose Filling System Malfunction

    FentaNYL citrate intravenous bags are recalled nationwide because a semi-automated filling system can malfunction and deliver double the intended dose. Patients and healthcare providers should immediately quarantine affected lots.

    Product
    FentaNYL citrate PF, 2500 mcg per 250 mL 0.9% Sodium Chloride (10 mcg per mL), Item F3342, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-072-82.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0863-2024·2024-02-07

    Smiths Medical Medfusion Model 3500 Syringe Pump Software Defects

    Smiths Medical recalls Medfusion Model 3500 syringe pumps (software versions before v6.0.0) due to multiple programming defects that could affect medication delivery rates, timing, and accuracy.

    Product
    smiths medical Medfusion Model 3500 Syringe pump
    Category
    Medical Device
    Distribution
    0 states