State
20,072 recalls have nationwide distribution and so reach Virginia. 0 additional recalls listed Virginia 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 Virginia 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.
Glenmark Pharmaceuticals is recalling Rufinamide 200mg tablets nationwide due to manufacturing process deviations. The voluntary recall affects certain lot numbers with July 2025 expiration dates.
Glenmark Pharmaceuticals is voluntarily recalling Voriconazole tablets nationwide due to manufacturing process deviations. No illnesses or injuries have been reported.
Glenmark Pharmaceuticals is recalling Ranolazine Extended-Release 1000mg tablets (Lot 17240040) nationwide due to manufacturing deviations. This is a voluntary, firm-initiated recall.
Glenmark Pharmaceuticals is recalling solifenacin succinate 10mg tablets nationwide due to manufacturing process deviations. The voluntary recall affects specific lot numbers distributed across the United States.
Glenmark Pharmaceuticals is voluntarily recalling Rosuvastatin Calcium 40mg tablets nationwide due to manufacturing practice deviations. The recall affects specific lot numbers expiring February through June 2026.
Glenmark Pharmaceuticals Inc. USA is recalling Clindamycin Hydrochloride Capsules, USP 300mg due to CGMP deviations. The product has been distributed nationwide.
Glenmark Pharmaceuticals is voluntarily recalling Cetirizine HCL 10mg tablets distributed nationwide. The recall was initiated due to Current Good Manufacturing Practice deviations.
BMW is recalling 2026 X6, X7, X5, and X5 Plug-In Hybrid models. The instrument panel may prevent the passenger-side airbag from deploying properly during a crash.
Ford is recalling certain 2024 Mustang vehicles because the brake pedal assembly may have been manufactured incorrectly, causing a loose brake pedal. A loose brake pedal can result in loss of braking function, increasing the risk of a crash.
Certain 2023-2024 RAM 2500 vehicles and related models have a faulty steering column control module that may cause turn signals and high beams to malfunction, increasing the risk of a crash. Owners should contact FCA US, LLC for free repairs.
Ford is recalling 2024-2025 Bronco and 2024 Ranger vehicles because the front upper control arm ball joint fastener may not be properly tightened or installed, potentially causing loss of steering control.
Long-Haul 5L ATV fuel containers sold on Amazon.com lack required child-resistant closures, posing burn, fire, and poisoning risks to children. About 815 units sold from January 2023 through October 2024 are recalled.
About 600 magnetic puzzle crab toys sold on Walmart.com are recalled because swallowed magnets can cause serious digestive injury. Consumers should stop using them immediately and request a full refund.
E-Bully youth ATVs sold online from 2023-2024 are recalled due to defective handlebars and brakes that can cause serious injury or death.
Suzuki is recalling 2022-2024 GSX1300R motorcycles for a brake master cylinder defect that can reduce stopping power and increase crash risk. Dealers will replace the affected components at no cost.
Costway recalls about 1,400 Babyjoy Convertible 6-in-1 High Chair Activity Centers sold online at Walmart.com due to leg openings that can trap children and a tray that can disengage, posing entrapment and fall hazards.
Fisher-Price is recalling about 15,300 Tissue Box Toys sold with 3-in-1 SnugaPuppy Activity Centers. The toy can detach and expose small brackets that pose a choking hazard to young children.
Fisher-Price is recalling about 253,000 Brunch & Go Stroller Toys because the egg component can crack and create choking hazards. No injuries have been reported; consumers should immediately stop use and request a free replacement.
Kramer Laboratories recalls Safetussin Max Strength Multi-Symptom Cough, Cold and Flu blister packs due to packaging that fails to resist child access. Tablets can be pushed through the foil, posing a poisoning risk to young children.
Kentfield Solid Wood Eight-Drawer Dressers can tip over if not wall-anchored, risking entrapment injuries or death to children. Modus Furniture is offering free repair kits and installation.
Bebamour baby bath seats pose a drowning risk because they are unstable and may tip over or allow babies to slip out. No injuries have been reported, but consumers should stop using them immediately.
Draeger's Anesthesia Circuit Kit Flex 2 is recalled because of the potential for cracks to form in the breathing circuit hose. No injuries have been reported.
Draeger, Inc. is recalling the Anesthesia Circuit Kit Flex 6 (Model MP02744) due to potential cracks forming in the breathing circuit hose. Approximately 293,660 units were distributed nationwide and internationally.
Draeger, Inc. is recalling 65,150 units of the VentStar Flex 220 breathing circuit due to the potential for cracks to form in the hose. A crack could affect gas delivery during anesthesia or ventilation procedures.
Draeger, Inc. is recalling the Anesthesia Circuit Kit Flex (P)2 due to the potential for cracks to form in the breathing circuit hose. This FDA Class I recall affects approximately 9,250 units distributed domestically and internationally.