State
73,092 recalls have nationwide distribution and so reach Connecticut. 6,571 additional recalls listed Connecticut specifically in their distribution scope.
Of the 6,571 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 1,590 (24%) are Severe.
Which agencies issued them
These figures cover only the 6,571 recalls whose distribution notice names Connecticut specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Sumitomo is recalling specific Falken WildPeak AT4W tires because they may contain incorrect cord material, increasing the risk of tire failure and crashes.
King Systems' KING LTSD oropharyngeal airway was marketed for pediatric use but lacked the required FDA clearance for that indication. Approximately 17,925 units were distributed nationwide.
Ambu is recalling VivaSight 2 DLT endotracheal tubes due to hyper angulation of the distal end, which increases risk of intubation complications and airway injury.
Integra LifeSciences is recalling surgical patties and strips due to higher-than-expected endotoxin levels in raw materials. The contamination may have resulted in out-of-specification finished products.
Integra LifeSciences is recalling Codman Surgical Patties and Strips because raw material contained higher-than-expected endotoxin levels, potentially affecting finished goods.
Dr. Reddy's Laboratories is recalling Cinacalcet 60 mg tablets nationwide because testing detected N-nitroso impurity exceeding FDA interim limits. The recall affects 35,880 bottles.
Integra LifeSciences' surgical patties and strips (Model 801404) are being recalled due to higher-than-expected endotoxin levels that may have resulted in out-of-specification products. No illnesses have been reported.
Integra LifeSciences is recalling surgical patties and strips due to higher-than-expected endotoxin levels in raw material, which may result in out-of-specification endotoxin in finished products.
West Pharmaceutical Services is recalling Vial2Bag Advanced 20mm Admixture Devices because heat exposure during shipping may have compromised the sterile barrier.
King Systems Corp. dba Ambu, Inc. is recalling 42,605 units of King LTSD Oropharyngeal Airways due to exceeding 510(k) exemption limitations.
King Systems Corp. is recalling KING LTSD airway kits (Model KKLTSD4325) because they were marketed for pediatric use without FDA approval for that indication. Approximately 36,727 units were distributed nationwide.
King Systems Corp. is recalling 31,457 units of King LTSD oropharyngeal airways because the device exceeded 510(k) exemption limitations by introducing a new pediatric indication.
Lucid is recalling 2024-2025 Air models due to a rear subframe wiring harness that may be too short, causing power loss to the rear drive unit and increasing crash risk. Replacement is free.
Tesla is recalling 2024 Cybertruck vehicles due to a drive inverter fault that may cause loss of propulsion. Affected owners will receive a free inverter replacement.
Kawasaki is recalling 2024 Ninja 7 Hybrid and Z7 Hybrid ABS motorcycles because a frame weld may crack, causing loss of control.
Polestar is recalling 2020 Polestar 1 vehicles because the brake pedal may detach from the brake booster, increasing crash risk.
Nova Bus is recalling certain 2010-2024 LFS buses because the driver's seat belt may not retract properly. This can result in a loose seat belt, increasing the risk of injury in a crash.
Continental Automotive is recalling MK C1 EVO brake systems where a fastener may be improperly assembled, causing the brake pedal to detach and increasing crash risk.
International is recalling 2024-2025 HX vehicles because insufficient lubricant in front axle hubs may damage wheel bearings, potentially causing wheel separation and loss of control.
Certain 2025 BMW X1 vehicles have B-Pillar reinforcement plates with insufficient structural strength. This defect may reduce crash protection and increase injury risk.
A2ZEV is recalling specific NACS to CCS1 charger adapters because a damaged locking mechanism can cause the charger to overheat, increasing the risk of personal injury.
KZRV is recalling 2025 Sportsmen 303QBSE travel trailers because the driver's side slide-out actuator is too close to the tires, posing a crash risk.
Forest River is recalling 2025 East to West Alta travel trailers because an incorrectly wired inverter may increase the risk of fire.
Winnebago Industries is recalling certain 2014-2025 RVs because hood bracket adhesive may have been incorrectly applied, allowing the bracket to detach and create a crash hazard. Dealers will provide free inspection and repair.
Forest River is recalling 2025 Vibe travel trailers because the stove may detach from the cabinet, increasing the risk of injury during use.