The Recall Desk

State

District of Columbia product recalls

73,104 recalls have nationwide distribution and so reach DC. 2,798 additional recalls listed District of Columbia specifically in their distribution scope.

What the numbers show

Total
2,798
Critical
240
Severe
948
Most recent
2026-09-23

Of the 2,798 recalls naming District of Columbia we have scored against our rubric, 240 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 948 (34%) are Severe.

These figures cover only the 2,798 recalls whose distribution notice names District of Columbia specifically. The 73,104 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10276–10300 of 75902

  • HighNHTSA·24V640000·2024-08-26

    Toyota Sequoia Hybrid tow hitch covers may come loose and detach

    Toyota is recalling certain 2023-2024 Sequoia Hybrid vehicles with a tow hitch cover attached to the rear bumper because the cover may come loose and detach from the vehicle.

    Product
    TOYOTA — TOYOTA SEQUOIA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V633000·2024-08-23

    Jaguar Recalls 2019 I-PACE Vehicles Due to High-Voltage Battery Overheating Risk

    Jaguar is recalling 2,760 2019 I-PACE vehicles because the high-voltage battery may overheat, increasing the risk of a fire. Owners should park outside and limit charging to 80% until repairs are complete.

    Product
    JAGUAR — JAGUAR I-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V637000·2024-08-23

    Great Dane Recalls 2025 Everest SS Trailers Due to Welding Defect

    Great Dane is recalling 2025 Everest SS refrigerated trailers because improperly welded support gear bracing mounts may cause the trailer to collapse.

    Product
    GREAT DANE — GREAT DANE EVEREST SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V634000·2024-08-23

    Ford fuel injectors assembled without O-ring support discs may leak

    Ford is recalling certain Lincoln Corsair, Escape, Mustang and Explorer vehicles because fuel injectors may have been assembled without O-ring support discs. 24 units affected.

    Product
    FORD — FORD, LINCOLN MUSTANG, ESCAPE, EXPLORER, CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24E073000·2024-08-23

    Navico Recalls Progressive RV Surge Protectors Due to Ground Contact Defect

    Navico Group is recalling Progressive RSM-30 and PSK-30 surge protectors for recreational vehicles because the ground contact may fail, increasing the risk of electrical shock.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V635000·2024-08-23

    Ford EcoBoost engine intake valves may break while driving

    Ford is recalling certain 2021-2022 vehicles with 2.7L or 3.0L Nano EcoBoost engines because the engine intake valves may break, resulting in engine failure and loss of drive power.

    Product
    FORD — FORD, LINCOLN EDGE, BRONCO, NAUTILUS, AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V629000·2024-08-22

    Salem and Wildwood trailer tires may contact chassis components and fail

    Forest River is recalling certain 2024-2025 Salem SBF325RL and Wildwood WBF325RL travel trailers because the tires may contact chassis components, causing tire failure.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24347·2024-08-22

    Head Rush Technologies TRUBLUE Speed Auto Belay Devices Fall Hazard

    Head Rush Technologies is recalling about 220 TRUBLUE Speed Auto Belay Devices because the backup brake can fail to activate, posing a fall hazard and risk of serious injury or death. Consumers should immediately stop using the devices and contact the manufacturer for a free inspection and repair.

    Product
    TRUBLUE Speed Auto Belay Devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V628000·2024-08-22

    Forest River trailer tires may contact the outrigger and fail

    Forest River is recalling certain 2024 Salem and Wildwood travel trailers because the tire may contact the outrigger, causing the tire to fail. 34 units are affected.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24348·2024-08-22

    Shawshank LEDz Squeeze Plush Ball Toys Recalled for Injury Hazard

    Shawshank LEDz is recalling approximately 9,600 Squeeze Plush Ball toys sold at Ace Hardware because the toys contain liquid and glitter that can splash out if the membrane ruptures, potentially injuring a child's eyes and face.

    Product
    Squeeze Plush Ball Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24346·2024-08-22

    Siemens SolarReady Meter Combos Recalled Due to Fire Hazard

    Siemens is recalling about 3,910 SolarReady Meter Combos because an interior connection can overheat and pose a fire hazard. The firm has received eight reports of overheating, including one localized fire, but no injuries.

    Product
    Siemens SolarReady Meter Combos
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2449-2024·2024-08-21

    Plum 360/A+ Spare Battery Defect Causes Accelerated Capacity Loss

    ICU Medical is recalling 130,826 units of Plum 360/A+ spare batteries due to a manufacturing defect that causes earlier-than-expected battery capacity loss and reduced runtime.

    Product
    Plum 360/A+ spare batteries. Item Number: SUB0000864.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2448-2024·2024-08-21

    Plum A+ and Plum A+3 Infusion Pump Batteries Recalled for Capacity Loss Defect

    ICU Medical is recalling Plum A+ and Plum A+3 infusion pump batteries due to a manufacturing defect that may cause premature capacity loss and reduced runtime. Approximately 14,744 units were distributed worldwide.

    Product
    Replacement Battery List Number SUB0000594 and SUB0000864 found in Plum A+ & Plum A+3 Infusion Systems, Pump List Numbers: 11005, 11971, 12391, 12618, 20678, 20679, 20792, 60529, 12348, 11973. OUS units marketed with the following descriptions: Plum A+ Mednet TM Firmware New…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2447-2024·2024-08-21

    Plum 360 Infusion Battery Recall Due to Manufacturing Defect

    ICU Medical is recalling Plum 360 Infusion System replacement batteries due to a manufacturing defect that may cause loss of capacity and decreased runtime earlier than expected. Approximately 11,961 units were distributed worldwide.

    Product
    Replacement Battery List Number SUB0000864, found in Plum 360 Infusion System, List Number 30010. Product description is PLUM 360 Infuser. OUS units marketed with the following descriptions: Bomba de infusi¿n Plum 360 compatible con el software ICU Medical MedNet, Plum 360…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V626000·2024-08-21

    Chevrolet Silverado rear bumper brackets may be insufficient for towing

    OEM Systems is recalling certain 2024 Chevrolet Silverado vehicles because the rear bumper mounting bracket may not be sufficient for towing, allowing a trailer to detach.

    Product
    CHEVROLET — CHEVROLET SILVERADO 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2579-2024·2024-08-21

    Merit Medical Convenience Kits Recalled for Syringe Leaks and Breakage

    Merit Medical is recalling medical convenience kits with defective syringes due to identified leaks, breakage, and quality issues that may pose a risk to patient health during procedures.

    Product
    Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Customer Procedure Kit (Angiography/Angioplasty kit), REF: K05-02166B K05T-00380C K05T-01674B K05T-01863 K05T-01941C K05T-01955 K05T-02138 K05T-02159 K05T-02272G…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2559-2024·2024-08-21

    Merit Medical catheter extractor kits recalled for syringe quality defects

    Merit Medical is recalling 3,631 catheter extractor convenience kits due to defective syringes with leaks and breakage. The identified quality issues may compromise patient safety during catheter removal.

    Product
    Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Outake, REF CET200 and CET300, The Catheter Extractor is a catheter accessory device intended for minimally invasive removal of tunneled long term catheters.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2558-2024·2024-08-21

    Merit Medical Convenience Kits with Recalled Syringes Pose Quality Risks

    Merit Medical is recalling convenience kits containing syringes with quality defects including leaks and breakage that may pose patient safety risks in cardiac and vascular procedures.

    Product
    Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Custom Procedure Kit (Angiography/angioplasty kit), REF: K12T-10773 K12T-09284D K12T-10621 K12T-10800 K12T-12491 To support various vascular or cardiac…
    Category
    Medical Device
    Distribution
    Distributed nationwide