State
72,820 recalls have nationwide distribution and so reach Connecticut. 6,564 additional recalls listed Connecticut specifically in their distribution scope.
Of the 6,564 recalls naming Connecticut we have scored against our rubric, 838 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,586 (24%) are Severe.
Which agencies issued them
These figures cover only the 6,564 recalls whose distribution notice names Connecticut specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Daavlin Distributing Company is recalling 26 Photera 600 phototherapy devices nationwide because the UV sensor gain calibration is incorrect, causing inaccurate ultraviolet output readings.
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.
Orthofix U.S. LLC is recalling Articulated Minirail Fixator external fixation devices due to incorrect model labeling. Three models were mislabeled: M101 labeled as M103, M103 labeled as M101, and M122 labeled as M111.
Bell Pharmaceuticals is recalling TopCare Earwax Removal Kit (Carbamide Peroxide 6.5%) because the drug is subpotent with significantly reduced active ingredient (~0.6% vs. expected 6–7%) and low pH. The affected product was distributed nationwide.
Bell Pharmaceuticals is recalling Audiologist's Choice Carbamide Peroxide earwax removal product due to subpotency: the active ingredient concentration is approximately 0.6% instead of the expected 6–7%, and the product has low pH.
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.
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.
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.
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.
Great Dane is recalling 2027 Champion dry van trailers because they may lack required rear impact guard extension channels, increasing injury risk in crashes.
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.
Foretravel is recalling 2027 Realm Presidential Motorcoaches because a fan assembly circuit board may overheat, increasing the risk of a fire.
Evenflo is recalling specific Reo by Revolve360 child seats because the headrest may shift during a crash, increasing injury risk.
Altec is recalling 2013-2025 AP45A trucks because a damaged wire in the cargo area can overheat and ignite flammable material, increasing the risk of fire.
International Motors is recalling 2025-2027 IC Bus CECB transit buses because driver's window and door joints may lack sufficient epoxy, failing federal safety standards.
SDADI Kitchen Step Stools, models LT01 and LT05, can collapse or tip over and allow children's bodies to fit through openings, creating serious injury and death risks. Consumers should stop using them immediately and contact the importer for a refund.
International Motors is recalling certain 2021, 2023–2027 MV and 2026–2027 HV vehicles. The battery interconnect cable may contact adjacent components, creating a short circuit that increases fire risk.
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.
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.
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.
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.