The Recall Desk

State

District of Columbia product recalls

20,199 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.

8651–8675 of 20199

  • HighFDA (Devices)·Z-2177-2024·2024-07-03

    Dental Scaler Tip May Not Seat Properly, Posing Injury Risk

    Dental EZ Group is recalling certain Titan Scaler Tip (Perio, Model 261669) units due to an oversized tip holder condition that may prevent proper seating, creating a risk of injury during use.

    Product
    Titan Scaler Tip - Perio Model/Catalog Number: 261669 The scaler tip is used with an air drive scaler for subgingival scaling and fine access. The Perio tip is used for lingual supragingival scaling of mandibular incisors and deep local pockets.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2185-2024·2024-07-03

    AXIOM Vertix Solitaire Medical Imaging Device Recall: Fire Risk from Power Supply Defect

    Siemens is recalling 4 AXIOM Vertix Solitaire medical imaging devices due to a short circuit in the touch display power supply that may cause overheating and fire. Units with serial numbers 1004, 1006, 1011, and 1014 are affected.

    Product
    AXIOM Vertix Solitaire - The Vertix MD Trauma has been specially designed for examining emergency and accident patients as well as for use in outpatient departments. Material Number: 8627718
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2201-2024·2024-07-03

    Medtronic MIRRO MRI implantable defibrillator recalled for weld defect

    Medtronic is recalling 3 MIRRO MRI DR SureScan implantable cardioverter defibrillators due to a manufacturing weld crack that caused devices to fail quality checks. The defect was detected during manufacturing before devices reached patients.

    Product
    MIRRO MRI DR SureScan, Model Number DDME3D1, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·24289·2024-07-03

    SWOMOG Children's Two-Piece Pajama Sets Recalled for Burn Hazard

    SWOMOG children's two-piece pajama sets sold on Amazon.com from May 2022 through January 2024 violate federal flammability standards for children's sleepwear, posing a burn hazard. Consumers should stop use immediately and contact SWOMOG for a full refund.

    Product
    SWOMOG Children's Two-Piece Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2219-2024·2024-07-03

    Stryker Hoffman LRF Wire Tensioner Adjustment Ring May Become Loose

    Stryker is recalling 39 Hoffman LRF Wire Tensioner devices because the adjustment ring may loosen, preventing proper tension setting. No injuries reported.

    Product
    Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2204-2024·2024-07-03

    Medtronic Implantable Cardioverter Defibrillator Recalled Due to Weld Crack Defect

    Medtronic is recalling 6 units of the MIRRO MRI VR SureScan implantable cardioverter defibrillator due to a potential manufacturing defect. The devices failed manufacturing quality checks because of a weld crack.

    Product
    MIRRO MRI VR SureScan, Model Number DVME3D1, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2174-2024·2024-07-03

    Blood Glucose Meter Recall: Accu-Chek Guide May Display Incorrect Measurement Units

    Roche is recalling Accu-Chek Guide (SC) blood glucose meters that may display readings in mmol/L instead of mg/dL, appearing approximately 18 times lower than actual. This could lead to incorrect treatment decisions and long-term diabetes complications.

    Product
    Accu-Chek Guide (SC) Kit -Intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip, palm, and upper arm as an aid in monitoring the effectiveness of glucose control. Product REF Number: 08453071001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V180000·2024-07-03

    2025 International LT vehicles recalled for reversed turn signal wiring

    Navistar is recalling certain 2025 International LT vehicles because two wires in the taillight jumper harness may be reversed, causing turn signals to activate in the wrong direction. This safety defect may confuse other road users and increase crash risk.

    Product
    INTERNATIONAL — 2025 INTERNATIONAL LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2188-2024·2024-07-03

    Siemens AXIOM Vertix Solitaire Display Fire Risk from Power Supply Short Circuit

    Siemens is recalling the AXIOM Vertix Solitaire diagnostic imaging component due to a short circuit in the Touch Display's power supply unit that may cause overheating and fire. Two units with serial numbers 1239 and 1241 are affected.

    Product
    ZE for Vertix Solitaire - The AXIOM Vertix Solitaire is a component and has been specially designed for examining emergency and accident patients as well as for use in outpatient departments Material Number: 5901900
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2203-2024·2024-07-03

    Implantable Cardioverter Defibrillator Recalled for Manufacturing Weld Defect

    Medtronic recalls 46 PRIMO MRI VR SureScan implantable cardioverter defibrillators due to a manufacturing defect. Weld cracks identified during manufacturing quality checks could cause device failure.

    Product
    PRIMO MRI VR SureScan, Model Number DVMD3D4, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2187-2024·2024-07-03

    X-ray table recalled for fire hazard from power supply unit short circuit

    Siemens MULTIX TOP I PRO X-ray tables are recalled due to a power supply short circuit that may cause overheating and fire. Three units have been identified.

    Product
    MULTIX TOP - Intended Use: The Multix TOP I PRO Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 475525
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2197-2024·2024-07-03

    Medtronic Implantable Cardioverter Defibrillator Recalled for Manufacturing Weld Defect

    Medtronic is recalling 14 units of EVERA MRI S VR SureScan implantable cardioverter defibrillators (Model DVMC3D4) due to potential weld cracks discovered during manufacturing. No patient injuries have been reported.

    Product
    EVERA MRI S VR SureScan, Model Number DVMC3D4, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·24291·2024-07-03

    Hatch Baby Power Adapters for Rest 1st Generation Sound Machines Pose Shock Hazard

    Hatch Baby is recalling power adapters sold with Rest 1st Generation sound machines because the plastic housing can detach from the adapter when unplugged, exposing electrical prongs and creating a shock hazard. The firm has received 19 reports of the housing coming off, including two reports of minor electrical shock.

    Product
    Power Adapters sold with Rest 1st Generation sound machines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2199-2024·2024-07-03

    Implantable Cardioverter Defibrillator with Weld Crack Defect Recalled

    Medtronic is recalling 40 EVERA MRI S DR SureScan ICDs (Model DDMC3D4) due to manufacturing weld cracks that caused devices to fail leak tests. The defect was identified during manufacturing; no patient harm has been reported.

    Product
    EVERA MRI S DR SureScan, Model Number DDMC3D4, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2192-2024·2024-07-03

    Medtronic Implantable Defibrillator Recalled Due to Manufacturing Weld Crack

    Medtronic is recalling 14 Cobalt XT HF CDT-D MRI SureScan implantable defibrillators due to a manufacturing weld defect that could cause device failure.

    Product
    Cobalt XT HF CDT-D MRI SureScan, Model Number: DTPA2D4, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·24288·2024-07-03

    American Honda Motor Recalls Off-Road Motorcycles for Grip Detachment

    American Honda Motor is recalling about 40,700 model year 2023-2024 off-road motorcycles (CRF50F, CRF110F, CRF125F) because the handlebar grip can detach, posing a crash and injury hazard. One crash resulting in a knee injury has been reported.

    Product
    Model Year 2023-2024 Off-Road Motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2193-2024·2024-07-03

    Implantable Defibrillator Recalled for Manufacturing Weld Crack Defect

    Medtronic is recalling 11 units of the COBALT XT HF QUAD CRT-D MRI SureScan implantable cardioverter defibrillator due to a manufacturing defect involving weld cracks that failed quality control testing.

    Product
    COBALT XT HF QUAD CRT-D MRI SureScan, Model Number DTPA2Q1, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2220-2024·2024-07-03

    CDC Influenza H5 Subtyping Kit may produce inconclusive test results

    The CDC Influenza A/H5 Subtyping Kit's H5b component may fail to amplify, resulting in inconclusive results. 191 units were distributed nationwide.

    Product
    CDC, Influenza A/H5 Subtyping Kit, Model/Catalog Number: FluIVD03-11
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2178-2024·2024-07-03

    Sonic Scaler Tip Holder May Be Oversized, Preventing Proper Seating

    The tip holder portion of Titan Blis-Sonic Scaler tips may be oversized, preventing proper seating in the scaler handpiece. This defect could result in the tip becoming loose during use.

    Product
    Titan Blis-Sonic Scaler packaged with the Titan Scaler Tip - Perio (part number 261669) (1) P/N 264563 (2) P/N 264565 The scaler tip is used with an air drive scaler for subgingival scaling and fine access. The Perio tip is used for lingual supragingival scaling of mandibu
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0569-2024·2024-07-03

    SinuFrin Nasal Decongestant Recalled for Sub-Potency Nationwide

    NeilMed Pharmaceuticals is recalling 20,370 bottles of SinuFrin Quick Relief Decongestant (Lot SD134) nationwide due to sub-potency. No illnesses have been reported.

    Product
    SINUFRIN QUICK RELIEF DECONGESTANT — SINUFRIN QUICK RELIEF DECONGESTANT (SINUFRIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·24V077000·2024-07-02

    2024 Kia Telluride recalled for engine valve spring failure

    Kia is recalling certain 2024 Telluride vehicles because engine valve springs may break while driving. This could cause loss of drive power and increased risk of fire.

    Product
    KIA — 2024 KIA TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V013000·2024-07-01

    2022 Chevrolet Equinox fuel pump module may cause engine stall

    General Motors is recalling certain 2021-2022 Chevrolet Equinox and 2022 GMC Terrain vehicles because the fuel pump module may not provide sufficient fuel to the engine, causing it to stall and increasing crash risk.

    Product
    CHEVROLET — 2022 CHEVROLET EQUINOX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·24744·2024-06-27

    Dania Furniture Recalls Hayden Bookcase Due to Tip-Over Hazard

    Dania Furniture is recalling about 940 Hayden Bookcases sold from November 2017 through February 2024 because the bookcase can tip over and cause entrapment injuries if not anchored to the wall. A 4-year-old child died from a tip-over incident in August 2023.

    Product
    Hayden Bookcase
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24285·2024-06-27

    Brookstone TurboVac Handheld Rechargeable Vacuums Recalled for Fire Hazard

    Southern Telecom is recalling about 10,600 Brookstone TurboVac handheld rechargeable vacuums (Model BSBVAC301) due to a fire hazard caused by battery short circuits during or after charging. The firm has received two reports of serious fires resulting in property damage.

    Product
    Brookstone TurboVac Handheld Rechargeable Vacuums
    Category
    Consumer Product
    Distribution
    Distributed nationwide