State
72,986 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 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Costway recalls about 1,400 Babyjoy Convertible 6-in-1 High Chair Activity Centers sold online at Walmart.com due to leg openings that can trap children and a tray that can disengage, posing entrapment and fall hazards.
Kramer Laboratories recalls Safetussin Max Strength Multi-Symptom Cough, Cold and Flu blister packs due to packaging that fails to resist child access. Tablets can be pushed through the foil, posing a poisoning risk to young children.
Volkswagen is recalling certain 2025 ID. Buzz vehicles because the brake system warning light may display the incorrect symbol and colour, failing FMVSS 135 and 101.
Forest River is recalling 2025 Coachmen Catalina travel trailers because the wastewater pipe may not extend to the exterior, allowing sewer gas to enter the cabin.
E-Bully youth ATVs sold online from 2023-2024 are recalled due to defective handlebars and brakes that can cause serious injury or death.
About 600 magnetic puzzle crab toys sold on Walmart.com are recalled because swallowed magnets can cause serious digestive injury. Consumers should stop using them immediately and request a full refund.
Long-Haul 5L ATV fuel containers sold on Amazon.com lack required child-resistant closures, posing burn, fire, and poisoning risks to children. About 815 units sold from January 2023 through October 2024 are recalled.
Bebamour baby bath seats pose a drowning risk because they are unstable and may tip over or allow babies to slip out. No injuries have been reported, but consumers should stop using them immediately.
Chrysler is recalling 2025 Ram 1500 vehicles because a software error may display incorrect tire pressure messages, increasing crash risk.
Forest River is recalling 2025 Coachmen Brookstone fifth wheels because a wastewater pipe defect may allow sewer gas to enter the cabin, increasing injury risk.
Draeger, Inc. is recalling the Anesthesia Circuit Kit Flex (P)2 due to the potential for cracks to form in the breathing circuit hose. This FDA Class I recall affects approximately 9,250 units distributed domestically and internationally.
Draeger's Anesthesia Circuit Kit Flex 2 is recalled because of the potential for cracks to form in the breathing circuit hose. No injuries have been reported.
Draeger's ID Circuit Flex 220 breathing circuit for anesthesia machines may develop cracks in the hose. The recall affects 3,325 units distributed nationwide and internationally.
McLaren is recalling certain 2020-2025 vehicles because brake lines may be routed incorrectly, activating the brakes on the wrong side and possibly locking a rear wheel.
Draeger, Inc. is recalling Anesthesia Circuit Kit Flex 1 devices nationwide and internationally due to potential cracks in the breathing circuit hose that conducts anesthesia gases.
Draeger, Inc. is recalling 65,150 units of the VentStar Flex 220 breathing circuit due to the potential for cracks to form in the hose. A crack could affect gas delivery during anesthesia or ventilation procedures.
Draeger, Inc. is recalling the Anesthesia Circuit Kit Flex 6 (Model MP02744) due to potential cracks forming in the breathing circuit hose. Approximately 293,660 units were distributed nationwide and internationally.
Draeger is recalling the Anesthesia Circuit Kit Flex EPA due to the potential for cracks to form in the breathing circuit hose. Approximately 13,620 units have been distributed domestically and internationally. Users should discontinue use of affected units immediately.
SeaBear Smokedhouse Salmon Chowder is recalled due to potential seal failure that could allow Clostridium botulinum contamination. The recall affects 11,152 pouches distributed nationwide.
Stryker Corporation recalls Otopore Cylinder outer ear wound dressing due to potential bubbles in blister seals that may breach the sterile barrier. Affected units were distributed nationwide.
Stryker's Nasopore 8cm nasal dressing is being recalled because packaging seals may have bubbles indicating the sterility barrier has been breached. The recall affects 182,344 units distributed nationwide.
Stryker Corporation is recalling 182,344 units of Hemopore nasal/sinus wound dressing due to potential packaging seal defects that could compromise sterility. A bubble on the blister seal may indicate the sterile barrier has been breached.
Stryker Corporation is recalling 182,344 units of Hemopore 2PK nasal/sinus wound dressing due to potential bubbles in blister seals that indicate sterility breach. Affected lot numbers are 2024020221, 2024051720, and 2024082321.
Reichert, Inc. is recalling 122 units of the Phoroptor VRx Digital Refraction System Model 16241 due to an assembly defect that could cause the device head to become loose and potentially detach.
Ethicon Endo Surgery recalls ETHIBOND EXCEL surgical sutures worldwide due to curing issues with the silicone coating on the needles identified during manufacturing.