The Recall Desk

State

District of Columbia product recalls

72,820 recalls have nationwide distribution and so reach DC. 2,795 additional recalls listed District of Columbia specifically in their distribution scope.

What the numbers show

Total
2,795
Critical
240
Severe
946
Most recent
2026-09-02

Of the 2,795 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 946 (34%) are Severe.

These figures cover only the 2,795 recalls whose distribution notice names District of Columbia specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

201–225 of 75615

  • SevereNHTSA·26V540000·2026-08-20

    Lucid Recalls 2022-2026 Air Vehicles Due to Fire Risk

    Lucid is recalling 2022-2026 Air vehicles because an electrical circuit may overheat, increasing the risk of fire or reduced visibility.

    Product
    LUCID — 2022 LUCID AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26712·2026-08-20

    Goal Zero Recalls YETI 3000X Power Stations for Fire and Burn Hazards

    Goal Zero is recalling about 46,200 YETI 3000X portable power stations because the circuit board can overheat, posing a risk of fire and burn injuries.

    Product
    Goal Zero YETI 3000X Portable Power Stations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26710·2026-08-20

    KTM Recalls GASGAS and Husqvarna Off-Road Motorcycles Due to Brake Defect

    KTM North America is recalling approximately 21,040 GASGAS and Husqvarna off-road motorcycles because the rear brake caliper can crack or break, posing a crash risk.

    Product
    GASGAS and Husqvarna Off-Road Motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26713·2026-08-20

    JINHEZO LED Tea Lights Recalled for Battery Ingestion Risk

    CPSC recalls JINHEZO Mini Waterproof LED Tea Lights because accessible button batteries pose a serious injury or death risk if swallowed.

    Product
    JINHEZO Mini Waterproof LED Tea Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26711·2026-08-20

    Modine Recalls Airedale Ventilation Fans in School Heat Pumps Due to Fire Hazard

    Modine is recalling Airedale ventilation fans in specific school heat pumps because water exposure can cause short circuits and fires. No injuries have been reported.

    Product
    Ventilation Fans in ClassMate® DX Cooling and Air Source Heat Pumps and SchoolMate® Water/Ground Source Heat Pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V538000·2026-08-20

    Rossmonster Recalls 2026 Motorcoaches Due to Rooftop Fan Fire Risk

    Rossmonster is recalling 2026 Baja, Skye, and Havn motorcoaches because a rooftop ventilation fan component may overheat and cause a fire.

    Product
    ROSSMONSTER — ROSSMONSTER BAJA, SKYE, HAVN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V568000·2026-08-20

    Ford F-650 SD Recall: Liftgate Platform Deck Pins May Break

    Marathon Industries is recalling one 2025 Ford F-650 SD because deck pins may break, causing the liftgate platform to fall and increasing injury risk.

    Product
    FORD — FORD F-650 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26C006000·2026-08-20

    Britax Recalls Infant Car Seats Due to Handle Detachment Risk

    Britax is recalling specific infant car seats because a screw in the carrying handle may come loose, causing the handle to partially detach and increasing the risk of a child falling.

    Product
    CHILD SEAT:HANDLE (INFANT) recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26714·2026-08-20

    Koorlian Mattresses Recalled for Fire Hazard Violating Flammability Standards

    CPSC recalls Koorlian mattresses sold on Amazon due to fire risks from violating mandatory flammability standards. Consumers should stop using them and contact the manufacturer for a free cover.

    Product
    Koorlian Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26716·2026-08-20

    CCM Hockey Recalls FMHVR Visors and ACCHVR Accessories Due to Laceration Risk

    CCM Hockey is recalling FMHVR Hybrid Visors and ACCHVR Replacement Visor Accessories because they can crack upon impact, posing a risk of laceration or impact injury.

    Product
    FMHVR Hybrid Visors and ACCHVR Replacement Visor Accessories
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0773-2026·2026-08-19

    Optiray Injection Recalled for Presence of Particulate Matter

    Liebel-Flarsheim is recalling 3,486 vials of Optiray Injection due to the presence of particulate matter, including plastic, stainless steel, and glass.

    Product
    OPTIRAY — OPTIRAY (IOVERSOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0772-2026·2026-08-19

    Victory Medical Center Pharmacy Recalls Glutathione Vials Due to Contamination

    Victory Medical Center Pharmacy is recalling 91 vials of Glutathione (MDV) 200 mg/mL due to bacterial endotoxin contamination.

    Product
    Glutathione (MDV), 200 mg/mL, 30 mL vial, each mL contains Glutathione 200 mg, Ascorbic Acid 20 mg, Benzyl Alcohol 1.5%, Na Hydroxide (Ph Adjust) in sterile water for injection, VMC.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0754-2026·2026-08-19

    Apollo Care Recalls Semaglutide Vials Due to Particulate Matter

    Apollo Care, LLC is recalling 250 vials of Semaglutide 5mg due to the presence of nylon and silk-type particulate matter.

    Product
    SEMAGLUTIDE 5mg (1mg/mL), Glycine 25 mg (5mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202.NDC 71170-712-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0787-2026·2026-08-19

    Baxter Recalls Cefazolin Injection Bags Due to Particulate Matter

    Baxter Healthcare is recalling 19,032 bags of Cefazolin Injection due to the presence of particulate matter. The affected product is distributed nationwide in the US.

    Product
    CEFAZOLIN — CEFAZOLIN (CEFAZOLIN SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2938-2026·2026-08-19

    Erbe ERBECRYO 2 Cryosurgical Unit Recalled Due to Rupture Risk

    Erbe USA Inc is recalling ERBECRYO 2 Cryosurgical Units because a strong pull on the high-pressure transfer hose may cause the cryoprobe to rupture.

    Product
    ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0752-2026·2026-08-19

    Apollo Care Recalls Semaglutide Vials Due to Particulate Matter

    Apollo Care, LLC is recalling 4,748 vials of Semaglutide 0.9mg due to the presence of nylon and silk particulate matter.

    Product
    SEMAGLUTIDE 0.9mg (0.9 mg/mL), 1 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-810-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0747-2026·2026-08-19

    Apollo Care Recalls Semaglutide Vials Due to Particulate Matter

    Apollo Care, LLC is recalling 56,918 vials of Semaglutide 12.5mg due to the presence of nylon and silk particulate matter.

    Product
    SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-495-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0748-2026·2026-08-19

    Apollo Care Recalls Semaglutide Vials Due to Particulate Matter

    Apollo Care, LLC is recalling specific lots of Semaglutide 2.25mg vials because they contain nylon and silk-type particulate matter.

    Product
    SEMAGLUTIDE 2.25MG (0.9 mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-811-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0757-2026·2026-08-19

    Apollo Care Recalls Semaglutide Vials Due to Particulate Matter

    Apollo Care, LLC is recalling specific lots of Semaglutide 20mg vials because they contain nylon and silk-type particulate matter.

    Product
    SEMAGLUTIDE 20mg (5mg/mL), Glycine 20 mg (5mg/mL), 4 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-724-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2920-2026·2026-08-19

    Dermalon Sutures Recalled for Potential Sterile Barrier Packaging Defects

    Covidien is recalling Dermalon 4-0 sutures because sterile barrier packaging may be perforated or torn, risking biocontamination and infection.

    Product
    Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31 DERMALON* 4-0 BLU 75CM C14 88861799-31
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0755-2026·2026-08-19

    Apollo Care Recalls Semaglutide Vials Due to Particulate Matter

    Apollo Care is recalling 250 vials of Semaglutide 7.5mg due to the presence of nylon and silk-type particulate matter.

    Product
    SEMAGLUTIDE 7.5mg (5mg/mL), Glycine 7.5 mg (5mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-721-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2922-2026·2026-08-19

    Surgipro II Sutures Recalled for Potential Sterile Barrier Defects

    FDA is recalling Surgipro II sutures due to potential sterile packaging defects that could cause biocontamination and infection.

    Product
    Surgipro II S8698GX SURGIPRO II BL 5/0 18 P-13 S8698GX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0749-2026·2026-08-19

    Apollo Care Recalls Semaglutide Vials Due to Particulate Matter

    Apollo Care, LLC is recalling specific lots of Semaglutide 6.75mg vials because they contain nylon and silk-type particulate matter.

    Product
    SEMAGLUTIDE 6.75mg (4.5 mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-821-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0753-2026·2026-08-19

    Apollo Care Recalls Semaglutide Vials Due to Particulate Matter

    Apollo Care, LLC is recalling 250 vials of Semaglutide 2.5mg due to the presence of nylon and silk particulate matter.

    Product
    SEMAGLUTIDE 2.5mg (1mg/mL), Glycine 12.5 mg (5mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-711-02
    Category
    Drug
    Distribution
    Distributed nationwide