State
73,584 recalls have nationwide distribution and so reach Connecticut. 6,572 additional recalls listed Connecticut specifically in their distribution scope.
Of the 6,572 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 1,881 (29%) are Severe.
Which agencies issued them
These figures cover only the 6,572 recalls whose distribution notice names Connecticut specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Truststone Group is recalling XO Poppy Power Trip Magnetic Wireless Power Banks because the lithium-ion batteries can overheat and ignite, posing fire and burn risks.
OKK Trading is recalling Rainbow Mystery Squishy Bun Toys because water beads inside can expand and cause choking or intestinal obstruction if swallowed.
Clorox is recalling about 6.3 million bottles of scented Mistolin and Lestoil cleaners sold in Puerto Rico and the U.S. Virgin Islands due to potential bacterial contamination.
SHEIN is recalling about 963 Spiral Toys because they contain small balls that pose a choking hazard to children under three.
Dreyer's Grand Ice Cream Inc. is recalling Outshine Strawberry Fruit Bars because they may contain glass pieces.
Mallinckrodt is recalling ACTHAR Gel vials due to the presence of glass and stopper pieces. Patients should stop using the product and contact their healthcare provider.
Medline is recalling neonatal and infant heated wire breathing circuits due to a risk of sporadic failure and thermal damage at the humidifier connector.
Dreyer's Grand Ice Cream Inc. is recalling Outshine Fruit Bars because they may contain glass pieces. Consumers should check for specific batch codes.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 50 mcg tablets nationwide because they may contain less than the labeled amount of active ingredient.
Dreyer's Grand Ice Cream Inc. is recalling Outshine Fruit Bars Grape due to the potential presence of glass pieces.
B. Braun Medical Inc. is recalling 23,688 bags of Lactated Ringer's Injection USP due to the presence of particulate matter.
Dreyer's Grand Ice Cream Inc. is recalling Outshine Tangerine Fruit Bars because they may contain glass pieces.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 100 mcg tablets because they may contain less active ingredient than labeled.
Medline is recalling 20 units of neonatal heated wire breathing circuits due to potential thermal damage that could cause airway obstruction or respiratory distress in infants.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium tablets because they may contain less active ingredient than labeled.
Accord Healthcare is voluntarily recalling Levothyroxine Sodium 300 mcg tablets because they may contain less active ingredient than labeled.
Dreyer's Grand Ice Cream Inc. is recalling Outshine Black Cherry Fruit Bars because they may contain glass pieces. Consumers should stop eating the product.
Dreyer's Grand Ice Cream Inc. is recalling Outshine Watermelon Fruit Bars because they may contain glass pieces.
Fresenius Kabi is recalling Tyenne (tocilizumab-aazg) injection vials because an internal investigation found the presence of glass particles.
Church & Dwight is recalling Zicam Cold Remedy Nasal Swabs because FDA inspections found out-of-limit microbiological testing results at the contract manufacturer.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 200 mcg tablets because they are subpotent. The recall covers distribution nationwide in the United States.
Philips is recalling Incisive CT scanners with specific software versions due to a potential failure to trigger clinical scans during bolus tracking.
Medline Industries is recalling 169 surgical convenience kits nationwide because they contain potentially contaminated components.
Healthmark Industries is recalling ProChek-II tests because they were manufactured with an expired ingredient, which may cause false negative or positive results.
Hollister is recalling specific lots of Onli hydrophilic urethral intermittent catheters because a manufacturing defect may cause a protrusion that leads to genitourinary trauma or bleeding.