The Recall Desk

State

District of Columbia product recalls

73,363 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 73,363 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

16876–16900 of 76161

  • HighFDA (Devices)·Z-1410-2023·2023-04-26

    Medtronic INFINITY Spinal Fusion Screws Recalled for Material Defect

    Medtronic is recalling 10 units of INFINITY Multi-Axial Screws distributed in the US and Canada because incorrect titanium material reduces gripping strength in affected lots.

    Product
    INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 32mm, REF 3604532; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical unction, the cervical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1419-2023·2023-04-26

    Beckman Coulter Free T3 Reagent Test Kit Recalled for Falsely Elevated Results

    Beckman Coulter is recalling Access Free T3 reagent test kits (Catalog #A13422, Lot #233968) because approximately 15-20% of samples produce falsely elevated results that could lead to misdiagnosis and inappropriate thyroid treatment.

    Product
    Beckman Coulter Access Free T3, Triiodothyronine, Free, Catalog #A13422, each box contains 2 reagent packs.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0733-2023·2023-04-26

    Dietary Supplement with Unapproved COVID-19 Treatment Claims Recalled

    Natural Solutions Foundation is recalling a colloidal silver dietary supplement labeled to treat COVID-19. The product violates FDA regulations prohibiting disease claims on dietary supplements.

    Product
    Dr. Rima Recommends The Silver Solution Immune System Support Dietary Supplement Nano Silver 10 ppm 16 fl. oz. (473 ml)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1391-2023·2023-04-26

    KLS E-Coupling Adapter Recalled for Incorrect Product Identifier Code

    Pro-Dex Inc is recalling 199 KLS E-Coupling Adapter devices due to incorrect Unique Device Identifier (UDI) and GTIN codes. The devices were distributed nationwide.

    Product
    KLS martin Group KLS E-COUPLING ADAPTER REF PDEC-1000-2 E-Coupling Adapter Assembly used to connect the KLS driver (e.g. drill) to a driver bit that fits into the adapter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1406-2023·2023-04-26

    Avanos Ballard Oral Care Swabs recalled for incorrect expiration date labeling

    Avanos Medical is recalling Ballard Oral Care Swabs (codes 12241, 12243, 12251) due to incorrect expiration date labeling. The recall affects 5,475 cases distributed worldwide.

    Product
    Avanos Ballard Oral Care Swab, Bulk Packed, Product Codes: a) 12241, b) 12243, c) 12251
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1396-2023·2023-04-26

    VITROS COVID-19 Antibody Test Calibrators Recalled for Incorrect Calibrator Levels

    Ortho-Clinical Diagnostics is recalling VITROS Anti-SARS-CoV-2 Total N Antibody Calibrators used in COVID-19 testing due to incorrect calibrator levels in Assay Data Disks, which can delay patient test results.

    Product
    VITROS Immunodiagnostic Products Anti-SARSCoV- 2 Total N Antibody Calibrators programmed onto the Assay Data Disks (ADD) Data Release Versions (DRV): DRVs 6213 through 6218 supporting VITROS Calibrators. Product Code: 6199976
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0537-2023·2023-04-26

    CVS Earwax Removal Drops Recalled for Subpotent Active Ingredient

    CVS-distributed earwax removal drops containing carbamide peroxide are being recalled because the active ingredient may degrade and become subpotent before the labeled expiration date, potentially leaving the product ineffective.

    Product
    Fast Acting Earwax Removal System (carbamide peroxide), 6.5%, 0.5 FL OZ (15 mL) Drops per bottle, OTC, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, CVS Product # 999532, UPC 0 50428 36475 8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1408-2023·2023-04-26

    Medtronic SenSight Extension Tunneler Kit: manufacturing defect prevents dual-extension passage

    Medtronic recalled approximately 1414 SenSight Extension Tunneler Kits due to a manufacturing defect where dual carriers were machined on only one side, preventing use for passing two extensions simultaneously.

    Product
    Medtronic SenSight Extension Tunneler Kit, REF B31030; The Extension Tunneler Kit is used to assist in the tunneling and passage of extensions for deep brain stimulation
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1398-2023·2023-04-26

    Pressure Therapy System Recalled for Unauthorized Deep Vein Thrombosis Prevention Claim

    Compass Health Brands is recalling the REX Pressure Therapy System because the user manual incorrectly claims the device can prevent deep vein thrombosis, an indication for which the device was not FDA-cleared.

    Product
    REX (Recovery Exercise X-Trainer) Pressure Therapy System- USER Manual. Intended to temporarily relieve minor muscle aches and/or pains, and to temporarily increase circulation to the treated areas. Models: DVTREX-U and DVTREX -L
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V292000·2023-04-25

    2023 Subaru Impreza Brake Light Switch and Transmission Interlock Defect

    Subaru is recalling certain 2023 Impreza vehicles due to a faulty brake light switch that may illuminate brake lights without pedal application and allow the transmission to shift out of PARK without pressing the brake pedal, creating rollaway and crash risk.

    Product
    SUBARU — SUBARU IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-04252023-01·2023-04-25

    Ivars Ready-to-Eat Meat Soup Products Subject to Public Health Alert

    USDA FSIS issued a public health alert for Ivars meat soup products prepared under insanitary conditions. Consumers should not eat these items.

    Product
    Ivars Commissary — FSIS Issues Public Health Alert for Ready-to-Eat Meat Soup Products Due to Possible Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·23V293000·2023-04-25

    2022 Indian Chief Dark Horse motorcycles recalled for missing belt guard reflectors

    Indian Motorcycle Company is recalling certain 2022 Indian Chief motorcycles that lack belt guard reflectors, which reduces visibility and increases crash risk. All affected vehicles have been remedied.

    Product
    INDIAN — INDIAN CHIEF BOBBER, CHIEF BOBBER DARK HORSE, CHIEF DARK HORSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V289000·2023-04-24

    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 — FOREST RIVER COLUMBUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E035000·2023-04-24

    Dana Spicer Ultimate Dana 60 Axle Recall for Jeep Wrangler

    Dana Incorporated is recalling Spicer Ultimate Dana 60 Bracketless Crate Axles for Jeep Wranglers because a suspension bracket may prevent sufficient lubrication from reaching the pinion tail bearings.

    Product
    POWER TRAIN:AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V288000·2023-04-24

    2023 Forest River Salem and Wildwood Travel Trailers: Brake Wiring Defect

    Forest River is recalling certain 2023 Salem and Wildwood travel trailers because the brakes may be incorrectly wired, resulting in potential loss of brake function and increased crash risk.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V291000·2023-04-24

    2022-2023 Nova Bus LFS Electric Bus Recalled for Battery Coolant Line Defect

    Nova Bus is recalling certain 2022-2023 LFS electric transit buses. The high voltage battery pack coolant line may not be fully seated, risking coolant loss and electrical short circuits that could cause fires.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V290000·2023-04-24

    Forest River Recalls 2023 East to West Travel Trailers for Placard Error

    Forest River is recalling 2023 East to West Della Terra and Silver Lake travel trailers because the Federal Placard may display incorrect weight and capacity data.

    Product
    EAST TO WEST — EAST TO WEST SILVER LAKE, DELLA TERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·014-2023·2023-04-21

    Abbyland Foods Recalls Frozen Turkey Sausage Patties Due to Undeclared Soy

    Abbyland Foods is recalling approximately 11,800 pounds of frozen turkey meatballs mislabeled as sausage patties because they contain undeclared soy.

    Product
    Abbyland Foods, Inc. — Abbyland Foods Recalls Frozen Turkey Sausage Patties Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V285000·2023-04-21

    2021-2024 Thor Motor Coach Motorhomes Recalled for Fuel Hose Defect

    Thor Motor Coach is recalling approximately 2,919 motorhomes with fuel hose clamps that may lack adequate clamping force, risking gasoline leaks and fires. Owners should contact dealers for free fuel hose and clamp replacement.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TELLARO, SEQUENCE, RIZE, SCOPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V286000·2023-04-21

    Motorhomes recalled for fuel hose defect in Cummins generators

    Certain 2021-2024 Forest River and Coachmen motorhomes equipped with Cummins Onan generators are affected by a fuel hose defect. The inadequate clamp force may cause a gasoline leak, increasing fire risk.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN SUNSEEKER, GALLERIA, NOVA, FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V287000·2023-04-21

    Shred-Tech Recalls MDS-4-33 Trucks Due to Fire Risk

    Shred-Tech is recalling 2021-2023 MDS-4-33 shredding trucks because paper accumulation can overheat and cause a fire.

    Product
    SHRED-TECH — SHRED-TECH MDS-4-33
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·012-2023·2023-04-20

    Weinstein Wholesale Meats Recalls Raw Ground Beef Burger Patties

    Weinstein Wholesale Meats is recalling raw ground beef burger patties due to possible contamination with white neoprene pieces.

    Product
    Weinstein Wholesale Meats Inc — Weinstein Wholesale Meats, Inc. Recalls Raw Ground Beef Burger Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·23V282000·2023-04-20

    International CV Brake Pressure Switch Fire Risk Recall

    Navistar is recalling 2017-2023 International CV trucks for a brake pressure switch assembly defect that may leak brake fluid and cause an electrical short-circuit, increasing fire risk while driving or parked.

    Product
    INTERNATIONAL — INTERNATIONAL CV
    Category
    Vehicle
    Distribution
    Distributed nationwide