State
73,503 recalls have nationwide distribution and so reach California. 13,262 additional recalls listed California specifically in their distribution scope.
Of the 13,262 recalls naming California we have scored against our rubric, 1,605 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,368 (25%) are Severe.
Which agencies issued them
These figures cover only the 13,262 recalls whose distribution notice names California specifically. The 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Walmart is recalling all lots of Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets nationwide. The product was marketed without FDA approval based on unapproved labeling claims.
Washington Homeopathic Products is recalling Tuberculinum Bovinum homeopathic remedy due to current good manufacturing practice deviations. No illnesses have been reported.
Washington Homeopathic Products is recalling Vaccinotoxinum homeopathic remedies (lot numbers 2512K and 20280) distributed nationwide due to cGMP manufacturing deviations. The voluntary recall was initiated by the firm in May 2022.
Washington Homeopathic Products recalls Colibacillinum homeopathic drug products due to manufacturing practice deviations. The recall involves 206 bottles distributed nationwide; the manufacturer voluntarily initiated it in May 2022.
Washington Homeopathic Products is recalling Morbillinum in multiple potencies due to manufacturing practice deviations. No illnesses have been reported.
AMS Packaging is recalling Premium Nature Instant Hand Sanitizer nationwide because FDA analysis found some bottles contain less ethanol than labeled.
Walmart Inc is recalling Artri King Reforzado con Ortiga Omega 3 Tablets nationwide because the product was marketed as a drug without FDA approval. All lots are affected.
Washington Homeopathic Products is recalling Tuberculinum homeopathic drug in multiple potencies due to manufacturing practice deviations. The voluntary recall affects product distributed nationwide.
Washington Homeopathic Products recalled Medorrhinum liquid pellets nationwide due to deviations from manufacturing standards. The product was distributed in 49 glass amber bottles.
Washington Homeopathic Products is recalling Pyrogenium homeopathic remedies in multiple potencies due to current Good Manufacturing Practice (cGMP) deviations. The firm initiated this voluntary recall affecting 6,782 bottles distributed nationwide.
Washington Homeopathic Products is voluntarily recalling Streptococcinum homeopathic drug in multiple potencies due to manufacturing practice deviations. No illnesses have been reported.
Washington Homeopathic Products is recalling Pertussinum in multiple potencies nationwide due to manufacturing practice deviations. Affected lot numbers are 18829, 20142, and 25410.
Washington Homeopathic Products is recalling Influenzinum in multiple potencies due to manufacturing process deviations. The recall affects approximately 6,400 units distributed nationwide.
Washington Homeopathic Products is recalling Syphilinum homeopathic products in multiple potencies due to current good manufacturing practice deviations. The affected products were distributed nationwide.
Washington Homeopathic Products is recalling Anthracinum liquid pellets due to manufacturing process deviations. The voluntary recall affects 219 bottles distributed nationwide.
Proterra is recalling 185 High Voltage Junction Box DC Links because a battery cable may not be properly connected, risking power loss, ground short circuits, or fire.
Fabform is recalling 2018-2022 FLR-D, FLRR-D, and DBX trailers because a rubber stop may break, allowing the utility gate to detach and increase crash risk.
Daimler Trucks North America is recalling 258 Thomas Built Buses and FCCC Saf-T-Liner models due to a software defect that may cause unexpected engine shutdowns, increasing crash risk.
Daimler Trucks recalls certain Thomas Built school buses (2020-2023) due to an engine control module defect that can cause unexpected engine shutdown while driving, increasing crash risk.
BorgWarner is recalling specific EGR valves where a loose washer may cause the valve to stick open, resulting in an unexpected loss of drive power.
Gillig is recalling 2019-2022 Low Floor electric buses because a cable connector may lose electrical connectivity, causing the vehicle to unexpectedly switch to Neutral.
Triple E is recalling 2021-2022 Unity and Wonder RVs because damaged burner control valves may cause a gas leak, increasing fire risk.
Heartland is recalling 2022 travel trailers because quick disconnect fittings in the LP gas system may crack, causing a gas leak that could lead to a fire. Dealers will replace the fittings free of charge.
Nova Bus is recalling one specific Sheppard model steering gear that may have been assembled incorrectly. The defect can cause the gear to fracture, leading to loss of steering control.
Cruiser RV is recalling 2022 travel trailers with potentially cracked LP gas system fittings that may leak, creating a fire hazard. Dealers will inspect and replace affected fittings free of charge.