State
72,940 recalls have nationwide distribution and so reach Connecticut. 6,566 additional recalls listed Connecticut specifically in their distribution scope.
Of the 6,566 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 1,588 (24%) are Severe.
Which agencies issued them
These figures cover only the 6,566 recalls whose distribution notice names Connecticut specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 2,840 VEVOR Garment Steamers are being recalled because they can leak or spit hot water. Reported cap failures resulted in two burn injuries, including a second-degree burn with permanent scarring.
About 2,650 Uuoeebb infant walkers are being recalled because they can fit through a standard doorway and fail to stop at the edge of a step, and their leg openings can entrap a child's head.
About 2,290 X-Pro Eagle and FRP Sahara 40cc youth ATVs are being recalled because their mechanical suspension fails safety requirements and the handlebars pose a laceration hazard.
General Motors is recalling 1,120 GMC Canyon AT4X AEV vehicles because incorrect sensing and diagnostic module software may cause a second stage passenger air bag deployment when only a first stage is intended.
About 8,960 YCXXKJ baby bath seats are being recalled because they are unstable and can tip over while in use, posing a risk of serious injury or death due to drowning.
About 700 model year 2026 Trek Domane+ and Checkpoint+ electric bicycles are being recalled because the chainring bolts can come loose, causing the chainring to separate from the bike.
BMW of North America is recalling 36,922 model year 2025-2026 X3 vehicles because unexpected steering wheel rotation may occur while the vehicle is stationary.
Lippert is recalling Q'Straint QRT-Max wheelchair restraints because the retractors may not lock, preventing proper securing of the wheelchair.
About 11,650 Vevor ice crushing machines are being recalled because they can experience a thermal event and ignite. Sanven has received two reports of thermal events, including one fire.
About 1,300 SKCAIHT children's mermaid costumes are being recalled because they contain a prohibited phthalate, violating the federal phthalates ban.
American Nuts is recalling 2,700 units of Dry Roasted Baking Macadamia Nuts over potential Salmonella contamination. The FDA has classified the action as Class I.
Genepro Protein is recalling 250 bags of Genepro Whey 4th Generation protein because the labeling contains incorrect ingredient information and fails to declare milk as an allergen.
Fresenius Kabi USA is recalling 483 cases of Ivenix LVP Primary Administration Sets after incorrect assembly of a specific lot that the firm states could result in serious patient injury.
Bridgestone is recalling Firestone Destination LE3 tires because a belt edge insert may be out of position, causing tread separation and increasing crash risk.
Lucid is recalling 2026 Gravity vehicles because incorrect seat covers may prevent side air bags from deploying correctly, increasing injury risk.
Blue Bird is recalling 2026-2027 Vision and All American school buses because wheelchair restraints may fail to lock, increasing injury risk.
Medtronic is recalling 6,591 Aurora EV-ICD and Clinical EV-ICD single chamber extravascular defibrillators over the potential for delayed time to high-voltage therapy in a rare sequence of events.
Philips North America is recalling the IntelliVue Patient Monitor MX750 over a potential issue where the monitors did not alarm.
Paragon 28 is recalling 20 Phantom Fibula Nails because out of specification thread depths may prevent the implant from mating with its mounting bolt, potentially requiring surgery to be aborted.
Philips North America is recalling the IntelliVue Patient Monitor MX800 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX600 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX500 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP20 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX450 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP40 over a potential issue where the monitors did not alarm.