State
73,596 recalls have nationwide distribution and so reach California. 13,263 additional recalls listed California specifically in their distribution scope.
Of the 13,263 recalls naming California we have scored against our rubric, 1,601 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,371 (25%) are Severe.
Which agencies issued them
These figures cover only the 13,263 recalls whose distribution notice names California specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Bell Pharmaceuticals is recalling Quality Choice Earwax Removal Kit (Carbamide Peroxide 6.5%) due to subpotent drug content, with assay levels significantly reduced (approximately 0.6% versus expected 6–7%) and low pH levels.
Papablic Inc is recalling Papablic Replacement Brush Heads (Model PAPA317AA) due to potential for brush heads to break. The recall affects approximately 13,400 packs distributed nationwide.
Bell Pharmaceuticals is recalling Good Neighbor Pharmacy Earwax Removal (Carbamide Peroxide 6.5%) due to subpotency—the active ingredient concentration is significantly reduced from expected levels, and the product has a low pH.
Daavlin Distributing Company is recalling Photera 600 3-D phototherapy devices because the UV sensor gain calculation is incorrect, causing inaccurate ultraviolet output measurement.
Bell Pharmaceuticals is recalling Meijer Earwax Removal Kit (Carbamide Peroxide 6.5%) due to subpotency: the product contains significantly reduced active ingredient (~0.6% vs. expected ~6–7%) and low pH, limiting effectiveness.
Medline is recalling 163 kits containing Zimmer Biomet mixing bowls and spatulas due to seal nonconformities that may compromise sterility. The defect could require extended surgery time to locate an alternative device.
Nutricia North America is recalling its NOURISH ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY because testing showed the product contains less vitamin A than the label states. A laboratory error led to inaccurate test results that overstated the actual vitamin A concentration in the product.
Daavlin Distributing Company is recalling the Photera 400 phototherapy device because the UV sensor calibration is calculating incorrectly, resulting in lower output levels than intended.
3B Medical, Inc. is recalling Rio II Nasal Pillows Interface devices due to packaging and labeling discrepancies involving product size identification and device identifiers. The affected models are RII1001 (Small), RII1002 (Medium), and RII1003 (Large).
Ford is recalling 76,748 2025-2027 Explorer and Lincoln Aviator vehicles because an unoccupied driver's seat may recline unintentionally, potentially trapping a second-row occupant.
Ember is recalling 2027 E-Series, Touring, and Overland travel trailers because the Federal Certification Label may list the wrong VIN, which could prevent owners from recognizing safety recalls.
Blue Bird is recalling 2022-2027 Vision transit buses because an exhaust hanger pin may damage the hydraulic brake line, causing leaks and increasing fire or crash risks.
Ford Motor Company is recalling certain 2021-2026 Bronco and Bronco Raptor vehicles because the engine compartment wiring harness may short circuit and cause a fire.
Blue Bird is recalling certain 2022-2027 Vision school buses because an exhaust hanger cotter pin may damage hydraulic brake lines, causing leaks that increase the risk of fire or crashes.
Altec is recalling 2024-2026 AT Series vehicles because turntable rotation bearing fasteners may not have been heat treated properly, posing a risk of component separation and injury.
Foretravel is recalling 2027 Realm Presidential Motorcoaches because a fan assembly circuit board may overheat, increasing the risk of a fire.
Turtle Top is recalling 2026 Terra Ford Transit buses because an electrical contactor may fail, preventing the wheelchair lift from stopping. This defect increases the risk of injury.
Evenflo is recalling specific Reo by Revolve360 child seats because the headrest may shift during a crash, increasing injury risk.
Great Dane is recalling 2027 Champion dry van trailers because they may lack required rear impact guard extension channels, increasing injury risk in crashes.
Currey & Company is recalling about 447 Nottaway chandeliers due to lack of proper electrical grounding, which poses a risk of serious injury or death from electrocution. Consumers should stop using them immediately and contact the company for a free replacement.
International Motors, LLC is recalling certain 2025-2027 IC Bus EVSB and CESB school buses due to insufficient epoxy coverage on body joints. This defect may cause panels to separate during a crash.
About 4,200 Liizousuda paint thinner bottles sold on Amazon lack child-resistant closures required by law. The product can cause serious injury or death if swallowed by young children.
MNIENT Adult Portable Bed Rails violate mandatory safety standards and pose risks of entrapment, asphyxiation, falls, and laceration. Consumers should stop using them immediately and contact the manufacturer for a refund.
Noerishia Adult Portable Bed Rails sold on Amazon violate the mandatory safety standard and pose a risk of serious injury or death from entrapment and asphyxiation. Users can become entrapped within the rail or between the rail and mattress.
Oitnlaughter LED Finger Lights sold on Amazon contain easily accessible button cell batteries that pose a risk of serious injury or death if swallowed by children. Consumers should stop using the toys immediately and contact Delightmi for a refund.