State
20,364 recalls have nationwide distribution and so reach DC. 0 additional recalls listed District of Columbia specifically in their distribution scope.
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.
General Motors is recalling certain 2022 Cadillac XT6, XT5, and GMC Acadia vehicles due to improperly tightened left-rear suspension toe links that may separate, potentially causing loss of vehicle control and crash risk.
Volvo is recalling 2022-2024 VNL and VHD trucks with RollTek driver seats due to a missing circuit that prevents side airbag deployment during a crash, increasing injury risk. Dealers will install a jumper harness for free.
IKEA is recalling about 25,000 BLÅVINGAD fishing games because a small metal rivet in a wooden play piece can come loose and pose a choking hazard to young children. Four incidents have been reported globally, with none in the U.S. requiring medical attention.
Monti Kids is recalling Basket with Balls toys sold in subscription boxes because the blue crocheted ball's sewn swirls can separate and expose small parts, creating a choking hazard for young children.
Navistar is recalling 2022-2023 International commercial vehicles with defective steering gears that may fracture and cause loss of steering control. Contact your dealer or Navistar at 1-800-448-7825 for inspection and free replacement.
BISSELL is recalling about 2,000 Cordless Multi-Surface Wet Dry Vacuums (models 2551R and 25518) because the battery pack circuit board can overheat and smoke, creating a fire hazard. No injuries have been reported.
Navistar is recalling 49 2023 International MV trucks because the driveshaft tube seam weld may separate or tear, causing sudden loss of drive power and increasing crash risk.
Mercedes-Benz USA is recalling approximately 218 2021 Cabriolet models due to rear headrests that may be incorrectly mounted to the seatbacks. The headrests could move or detach during a crash, increasing the risk of injury.
Daimler Trucks North America is recalling approximately 17 certain 2022 Freightliner Cascadia trucks because the antilock brakes and electronic stability control can be manually disabled, violating federal safety standards and increasing crash risk. The company will repurchase affected vehicles.
Instrumentation Laboratory recalled ACL ELITE refurbished coagulation analyzers to remove the HemosIL Liquid Anti-Xa test definition.
The Express Mini 500 Dry Seal Chest Drain has been recalled because its instructions do not adequately warn against draining it for continued use or using it outside healthcare settings. Approximately 8,184 cases were distributed worldwide.
PJ Trailers is recalling certain 2022-2024 trailers with Demco EZ Latch Gooseneck Couplers because the mounting bolts may loosen, causing the coupler to separate and creating a crash risk.
Jaguar Land Rover is recalling 2022-2023 Range Rover vehicles because the second-row armrest latch may fail, allowing unsecured objects to strike occupants during a crash. Dealers will replace the locking arm free of charge.
Direct Rx is voluntarily recalling Glimepiride 2 mg tablets nationwide due to manufacturing practice violations. The recall affects multiple lot numbers of 30-count and 90-count bottles distributed across the United States.
Preat Corp is recalling Neodent GM X 6mm titanium base components due to a dimensional defect causing vertical movement. This instability may lead to abutment fracture and potential ingestion of dental materials by patients.
Siemens ARTIS pheno X-ray systems may experience unintended table movement that the system fails to detect, risking injury to patients, staff, or operators. The FDA is recalling 141 affected units nationwide.
Entopsis, Inc. is recalling PCRopsis Reagent RVD-RT diagnostic kits due to misleading label statements that could affect proper use and test interpretation.
Ascend Laboratories is recalling 12,804 bottles of Dabigatran Etexilate 150mg capsules nationwide due to detection of N-nitroso-dabigatran (NDAB) impurity levels above the Acceptable Daily Intake limit caused by manufacturing process deviations.
Direct Rx is recalling Ropinirole 1 mg tablets nationwide due to manufacturing process deviations. Consult a pharmacist before stopping this medication.
The Atrium Pneumostat Chest Drain Valve has been recalled because its instructions lack sufficient precautions against improper drainage and use outside healthcare settings.
Elekta Instrument AB is recalling 70 Leksell Stereotactic System neurosurgical devices due to incorrect Instructions for Use being distributed with the devices. Incorrect documentation for neurosurgical equipment could impact proper device use.
Instrumentation Laboratory is removing the HemosIL Liquid Anti-Xa test definition from ACL Elite/Elite Pro Analyzers. This affects 358 units in the US and 558 units internationally.
Jayco is recalling 2024 Entegra Vision and related motorhomes due to rear brake caliper attachment bolts that may not be properly tightened. Loose bolts could damage the wheel or brake lines, reducing brake performance and increasing crash risk.
BINDLE BOTTLE is recalling Stainless Steel Water Bottles because the cup's screw cap is attached by a weld that leaches lead into drinking water.
Daimler Trucks is recalling commercial trucks with incorrect weight-rating labels that could allow unsafe overloading. Dealers will replace the labels free of charge.