State
72,820 recalls have nationwide distribution and so reach New York. 12,890 additional recalls listed New York specifically in their distribution scope.
Of the 12,890 recalls naming New York we have scored against our rubric, 1,501 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,131 (24%) are Severe.
Which agencies issued them
These figures cover only the 12,890 recalls whose distribution notice names New York specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Daikin Comfort Technologies is recalling Amana Through-The-Wall air conditioners and heat pumps because a shorted component can cause fire and serious injury.
Gizoon Direct is recalling six-drawer double dressers due to tip-over and entrapment risks that can cause serious injury or death to children.
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.
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.
Branch is recalling about 16,000 ergonomic chairs because the backrests can detach, posing a fall hazard. No injuries have been reported.
SHEIN is recalling about 963 Spiral Toys because they contain small balls that pose a choking hazard to children under three.
OKK Trading is recalling Rainbow Mystery Squishy Bun Toys because water beads inside can expand and cause choking or intestinal obstruction if swallowed.
Skip Hop is recalling Baby Sesame Street Elmo Silicone Teethers because the black eyes can detach if frozen, posing a choking risk.
CPSC recalls GIHNJSI Squeezy Dumplings toys sold on Amazon due to water beads that pose serious ingestion, choking, and obstruction hazards.
Nova Bus is recalling Casco engine coolant level sensors that may send false signals, causing unexpected engine shutdowns and increasing crash risk.
Dreyer's Grand Ice Cream Inc. is recalling Outshine Watermelon Fruit Bars because they may contain glass pieces.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium tablets because they may contain less active ingredient than labeled.
Dreyer's Grand Ice Cream Inc. is recalling Outshine Fruit Bars Grape due to the potential presence of glass pieces.
Fresenius Kabi is recalling Tyenne (tocilizumab-aazg) injection vials because an internal investigation found the presence of glass particles.
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 Strawberry Fruit Bars because they may contain glass pieces.
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 Levothyroxine Sodium 300 mcg tablets because they may contain less active ingredient than labeled.
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.
Medline is recalling neonatal and infant heated wire breathing circuits due to a risk of sporadic failure and thermal damage at the humidifier connector.
B. Braun Medical Inc. is recalling 23,688 bags of Lactated Ringer's Injection USP due to the presence of particulate matter.
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.
Church & Dwight is recalling Zicam Cold Remedy Nasal Swabs because FDA inspections found out-of-limit microbiological testing results at the contract manufacturer.