The Recall Desk

State

District of Columbia product recalls

20,096 recalls have nationwide distribution and so reach DC. 0 additional recalls listed District of Columbia specifically in their distribution scope.

About recalls in District of Columbia

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect District of Columbia consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

6726–6750 of 20096

  • SevereNHTSA·24V433000·2024-12-06

    2025 Kenworth and Peterbilt Trucks Steering Linkage Defect

    PACCAR is recalling 2025 Kenworth and Peterbilt trucks due to improperly heat-treated ball studs in steering assemblies that may break, causing loss of steering control.

    Product
    KENWORTH — 2025 KENWORTH W990
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25061·2024-12-05

    Belkin Power Bank Recalls Due to Fire Hazard from Battery Overheat

    Belkin is recalling about 4,000 BoostCharge Pro wireless charger power banks due to a fire hazard from overheating lithium-ion batteries. One unit caught fire and damaged a house.

    Product
    Belkin BoostCharge Pro Fast Wireless Charger Power Banks 10K
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25056·2024-12-05

    Anker Soundcore and PowerConf Bluetooth speakers recalled for fire hazard

    Anker is recalling about 69,000 Soundcore and PowerConf Bluetooth speakers sold on Amazon in 2023 due to overheating lithium-ion batteries. The firm received 33 reports of incidents, including fires and one minor burn injury.

    Product
    Anker Soundcore (A3102) and PowerConf Bluetooth (A3302) Speakers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25058·2024-12-05

    NetZero High Bay LED Fixtures Recalled Due to Fire Hazard

    NetZero USA is recalling about 13,000 High Bay LED light fixtures due to plastic pin degradation that can cause the LED board to come loose and catch fire. Seven burning incidents have been reported with no injuries.

    Product
    High Bay LED light fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25057·2024-12-05

    Scented candles recalled due to fire and laceration hazards

    Vacation Inc. recalls about 13,000 units of Black Label Scented Candles due to flame overheat causing glass breakage and creating fire and laceration risks. No injuries have been reported, but consumers should stop using the product immediately.

    Product
    The Legendary 'VACATION' by Vacation Black Label Scented Candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V365000·2024-12-05

    Loose Seat Belt Attachment in Winnebago and Itasca Motorhomes

    Winnebago and Itasca recall certain 2020-2023 motorhomes due to improperly tightened seat belt attachments that may fail to restrain occupants in a crash. Dealers will tighten fasteners free of charge.

    Product
    WINNEBAGO — 2021 WINNEBAGO INSPIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25059·2024-12-05

    QVC recalls 1.1 million Temp-tations oven gloves due to burn hazard

    QVC is recalling about 1.1 million pairs of Temp-tations oven gloves that can fail to protect from heat, causing a burn hazard. The company received 162 reports of insufficient protection, including 92 reports of minor burns.

    Product
    Temp-tations Oven Gloves
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25703·2024-12-05

    Polaris RZR XP Off-Road Vehicles Recalled Due to Fire Hazard

    Polaris is recalling about 21,000 RZR XP 1000 and XP 4 1000 recreational off-road vehicles because the battery terminal cover can be damaged by the seat base, exposing the battery post and creating a fire hazard. No injuries have been reported.

    Product
    Model Year 2024-2025 RZR XP 1000 and XP 4 1000 ROVs
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25060·2024-12-05

    Fireproof Gun Safes Recalled for Locking Mechanism Failure Risk

    Academy Sports + Outdoors is recalling about 6,100 Redfield 12- and 18-gun fireproof safes because mechanical locking plates can fail, potentially allowing unauthorized access. No injuries have been reported.

    Product
    Redfield 12- and 18-Gun Fireproof Safes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25702·2024-12-05

    Polaris Recalls 2024 Ranger and Bobcat Off-Road Vehicles for Seat Belt Defect

    Polaris recalled about 2,500 Model Year 2024 Ranger and Bobcat vehicles with a defective passenger side seat belt anchor weld. Consumers should immediately stop carrying passengers and contact an authorized dealer for free repair.

    Product
    Model Year 2024 Ranger Recreational Off-Road Vehicles (ROVs) and ProXD and Bobcat Utility Task Vehicles (UTVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0328-2025·2024-12-04

    Hologic BioZorb Radiographic Marker Recalled Due to Serious Injury Reports

    Hologic has recalled 12,710 BioZorb Markers nationwide after receiving reports of serious complications including infection, device migration, and device erosion. The FDA classified this as a Class I recall.

    Product
    BioZorb Marker. Radiographic soft tissue marker.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V289000·2024-12-04

    2022 Forest River Columbus fifth wheel: missing riser tube risks tire damage and crashes

    Forest River is recalling approximately 137 2022 Columbus fifth wheel vehicles because the riser tube between the axle hangers was not installed. This creates inadequate tire clearance, risking tire puncture and vehicle crashes.

    Product
    FOREST RIVER — 2022 FOREST RIVER COLUMBUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0515-2025·2024-12-04

    MEDLINE Epidural Procedure Kits: Connector May Prevent Catheter Insertion

    MEDLINE epidural trays used for labor anesthesia may have connectors that fail to fully open, preventing proper catheter insertion. The recall affects 2,592 units distributed across the US and internationally.

    Product
    MEDLINE procedure kits labeled as follows: 1) L&D CONTINUOUS EPIDURAL TRAY, REF PAIN1699; 2) L&D CONTINUOUS EPIDURAL TRAY, REF PAIN1699A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0539-2025·2024-12-04

    Philips Breast MRI System Recalled for Patient Safety Risk

    Philips is recalling 5,231 units of the dS Breast 7ch 1.5T breast MRI system due to a potential safety issue that could harm patients during preparation or scanning.

    Product
    dS Breast 7ch 1.5T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0518-2025·2024-12-04

    GE SIGNA Architect MRI Systems Recalled for Elevated Acoustic Noise

    GE Medical Systems is recalling certain SIGNA Architect MRI systems because their gradient coils can produce elevated acoustic noise during scanning under specific conditions, potentially risking hearing damage.

    Product
    SIGNA Architect, Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0152-2025·2024-12-04

    Treehouse Foods Recalls Frozen Waffles for Potential Listeria Contamination

    Treehouse Foods is recalling BREAKFAST BEST frozen griddle waffles nationwide due to potential Listeria monocytogenes contamination. Approximately 9.9 million cases are affected; consumers should not eat the product.

    Product
    BREAKFAST BEST 12/12.3oz MXD CS GRDL WFL PMPKN/CINN-BKBST UPC 4061463257208
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·24V267000·2024-12-04

    Ford Bronco Sport Control Module Failure May Disable Drive Power

    Ford is recalling Bronco Sport and Maverick models due to control module defects that may fail to detect low battery charge, potentially disabling drive power and increasing crash risk. Dealers will provide free recalibration.

    Product
    FORD — 2022 FORD BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0517-2025·2024-12-04

    Discovery MR750w MRI Scanner Recalled for Elevated Acoustic Noise

    GE Medical Systems is recalling 8 Discovery MR750w 3.0T MRI scanners because their gradient coils can produce elevated acoustic noise during scanning under specific conditions.

    Product
    Discovery MR750w 3.0T, whole body magnetic resonance scanner
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0193-2025·2024-12-04

    Griddle Waffles with Flax Recalled Due to Listeria Contamination Risk

    Multiple brands of organic griddle waffles with flax are being recalled due to potential Listeria monocytogenes contamination. Affected products include Wegmans, H-E-B, Nature's Path Organic, and Central Market brands.

    Product
    WEGMANS 12/7.4oz GRDL WFL FLAX ORG - WEGMN UPC 077890481424 H-E-B 12/8.25oz GRDL WFL FLAX ORG-HEBUT UPC 041220708338 WEGMANS 12/8.25OZ 6CT GRDL WFL FLAX ORG-WEGMN UPC 077890577059 NATURES PATH ORGANIC 12/7.4oz GRDL WFL FLAX ORG - NPTHO UPC 058449590569 NATURES PATH ORGANIC 12/210
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0189-2025·2024-12-04

    Kodiak Cakes Griddle Waffles Recalled for Potential Listeria Contamination

    Treehouse Foods is recalling Kodiak Cakes 8/10.72oz Griddle Waffles with Chocolate Chip due to potential Listeria monocytogenes contamination. The recall affects approximately 9,907,389 cases distributed nationwide in the United States and Canada.

    Product
    KODIAK CAKES 8/10.72oz GRDL WFL CHOC CHIP-KDKCS UPC 705599013201
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0150-2025·2024-12-04

    Treehouse Foods Plant-Based Waffles Recalled for Listeria Contamination Risk

    Treehouse Foods is recalling BREAKFAST BEST plant-based waffles nationwide due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and best-by dates from October 2024 through October 2025.

    Product
    BREAKFAST BEST 12/8 OZ GRDL HSTYLE PLNT BSD WFL-BKBST UPC 4061459885750
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0191-2025·2024-12-04

    Griddle Waffles Recalled for Potential Listeria Contamination

    Multiple brands of cinnamon griddle waffles are being recalled due to potential Listeria monocytogenes contamination. Approximately 9.9 million cases are affected.

    Product
    WESTERN FAMILY 12/280g GRDL WFL CIN - WSTCN UPC 062639310134 GREAT VALUE 12/280g GRDL WFL CIN - GRVLC UPC 681131811712 SELECTION 12/280g GRDL WFL CIN - SLCTN UPC 059749950640 COMPLIMENTS 12/280g GRDL WFL CIN - CMPLM UPC 055742500516 KROGER 12/12.3oz GRDL WFL CIN - KROGR UPC 01111
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0214-2025·2024-12-04

    Breakfast Best Griddle Waffles Recalled for Potential Listeria Contamination

    Treehouse Foods is recalling approximately 9.9 million cases of Breakfast Best griddle waffles for potential Listeria monocytogenes contamination. Consumers should discard the product or return it to the retailer.

    Product
    BREAKFAST BEST 12/12.3oz GRDL WFL CHOC PEP MOCHA-BKBST UPC 04061463991591
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0535-2025·2024-12-04

    VITROS Chemistry CRP Diagnostic Slides May Underreport Elevated Results

    Ortho-Clinical Diagnostics is recalling 7,717 units of VITROS CRP diagnostic slides that may produce falsely low results for high C-reactive protein samples, risking missed diagnosis of infection or inflammation.

    Product
    VITROS Chemistry Products CRP Slides- In vitro diagnostic quantitatively measures C-reactive protein (CRP) concentration in serum and plasma Model/Catalog Number: 1926740
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0549-2025·2024-12-04

    Offset Cup Impactor Surgical Instruments Recalled for Weld Fracture

    INCIPIO DEVICES is recalling 100 units of Offset Cup Impactor surgical instruments (Lot 24A0087) because the TIG weld does not meet specifications and has fractured. These instruments are used in hip surgery to position acetabular cup implants.

    Product
    Offset Cup Impactor - 3/8-16 interface. Reusable surgical instrument used to position and place acetabular sup implants.
    Category
    Medical Device
    Distribution
    Distributed nationwide