State
19,713 recalls have nationwide distribution and so reach Connecticut. 0 additional recalls listed Connecticut specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Connecticut consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
BMW is recalling certain 2025–2026 BMW X1 and X2 vehicles, along with MINI Cooper and Countryman models, because the front seat belt retractors may be damaged and fail to properly restrain occupants during a crash.
EEMB lithium coin battery packs sold online are not in child-resistant packaging as required by law. If swallowed by a child, these batteries can cause serious internal injuries or death.
Svnntaa bed rails sold on Amazon violate safety standards and pose a risk of entrapment, asphyxiation, falls, and laceration. Consumers should stop using them immediately and contact Eokeanon for a refund.
Analemma Water Bottles are recalled because the inner glass liner can break, posing risk of serious injury or death from laceration and ingestion. The importer has received 20 reports of the glass breaking, including one oral injury.
Allura Imports is recalling about 120 youth sweatshirts with drawstrings due to risk of strangulation. The drawstrings can catch on objects and cause serious injury or death to children.
Pending LLM rewrite. Source: NHTSA 25V474000.
Pending LLM rewrite. Source: NHTSA 25V472000.
Pending LLM rewrite. Source: NHTSA 25V473000.
EVLWZL and Gunugu mattresses violate mandatory flammability standards and pose a risk of serious injury or death from fire. Approximately 670 units sold through Amazon, Walmart, and Wayfair from October 2025 through March 2026 are affected.
Pending LLM rewrite. Source: NHTSA 25V471000.
Multi-purpose helmets sold on Temu by Foubeaka and Geniuss are recalled because they violate mandatory bicycle helmet safety standards and can fail to protect users in a crash, posing a serious risk of injury or death.
Natural Pigments is recalling about 860 bottles of Rublev Colours Gum Turpentine and Mineral Spirits due to non-compliant packaging that poses a risk of serious injury or death from child poisoning.
The CPSC has recalled Justforjoyful Rainbow Wall Toys because the drumstick attached to the xylophone component has a spherical end that violates the mandatory children's toy safety standard and poses a choking hazard. About 160 units were sold on Amazon from December 2025 through March 2026.
ZMC Group is recalling about 124,560 battery-operated light-up toys because they contain easily accessible button cell batteries that can cause serious internal injuries or death if swallowed by children. Consumers should stop using the toys immediately and contact the manufacturer for a refund.
Favoto Model H-1 bike helmets violate mandatory safety standards and may fail to protect users in a crash, posing a risk of serious head injury or death. About 2,200 units sold on Amazon from April 2022 through January 2026 are affected.
Scope Health is recalling Optase Dry Eye Intense Drops (Glycerin 0.2%) due to lack of assurance of sterility. The product is distributed nationwide.
Beta Bionics is recalling iLet Bionic Pancreas units with software versions 1.4.2 and 1.4.3 due to a compatibility issue with Dexcom G7 sensors that can cause delayed glucose readings and loss of automatic insulin adjustments.
Immuno-Mycologics, Inc. is recalling Immy Myco DDR Trident Bulk Neutralization Buffer B (60 X 30 mL, Lot F5061154) because the product may contain contaminants. The buffer is used for clinical specimen processing for Mycobacterium spp. diagnosis.
Alcon Research LLC is recalling GenTeal Tears Lubricant Eye Gel nationwide due to FDA inspection observations indicating the product may lack assurance of sterility. Consumers should not use affected lots.
Alcon Research LLC is recalling Systane Lubricant Eye Gel Night Gel (10g) distributed nationwide due to FDA inspection observations regarding lack of assurance of sterility that may impact product quality.
Abbott is recalling certain i-STAT EG6+, EG7+, and G3+ blood gas cartridges that may report falsely high CO2 and falsely low pH results due to a manufacturing issue, potentially leading to unnecessary or harmful clinical interventions.
DePuy Synthes is recalling one lot of ATTUNE Revision Hinge Femoral components (left size 7, part number 150450107) due to external sterile packaging adhered to internal packaging, potentially compromising product sterility.
Depuy Synthes is recalling 3 units of the ATTUNE Revision Hinge Femoral (Right, Size 5, Cemented) knee implant due to external sterile packaging adhered to internal sterile packaging, potentially compromising product sterility.
Abbott Point Of Care is recalling approximately 7.6% of specific i-STAT EG7+ cartridge lots due to a manufacturing issue causing falsely high pCO2 and low pH readings. Inaccurate results could lead clinicians to make unnecessary or harmful medical interventions.
Pending LLM rewrite. Source: FDA_FOOD H-0684-2026.