State
72,907 recalls have nationwide distribution and so reach Alaska. 1,764 additional recalls listed Alaska specifically in their distribution scope.
Of the 1,764 recalls naming Alaska we have scored against our rubric, 118 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 350 (20%) are Severe.
Which agencies issued them
These figures cover only the 1,764 recalls whose distribution notice names Alaska specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 2,200 BABESIDE doll and stroller toy sets are being recalled because the small pacifier violates the small parts ban and the plush bear's eyes can detach.
About 1,060 Pyro Diablo "Diablo Rising" 9 Shots fireworks devices are being recalled because their pyrotechnic composition exceeds the federal limit.
Veseacky children's pajama sets are recalled due to burn hazards from violating mandatory safety standards for children's sleepwear. About 3,700 units were sold on Amazon from October 2020 through January 2026.
Farber Specialty is recalling 2025-2026 HX620 and MCXCR emergency vehicles because the touchscreen may fail, preventing the activation of exterior lights and emergency equipment.
About 2,355 CooCooBaby Classic and Deluxe Baby Loungers are being recalled for violating the mandatory standard for infant sleep products, posing a suffocation hazard.
About 5,000 Arizer Solo III Intergalactic (Black) portable vaporizers are being recalled after four reports of the internal lithium-ion battery exploding or igniting.
General Motors is recalling 2026–2027 Cadillac Vistiq vehicles because the third-row power seatback may fail to reverse when it encounters a person, potentially trapping them.
Beekeeper's Naturals Saline Nasal Spray with propolis and xylitol, 1 fl oz, is being recalled for microbial contamination of non-sterile products. 1,680 bottles are affected.
Doxorubicin Hydrochloride Liposome Injection, 50 mg/25 mL single-dose vials, is being recalled because of particulate matter identified as glass. 675 vials are affected.
TNVitamins and Doctor's Pride moringa green superfood capsules are being recalled because the product may be contaminated with Salmonella. 13,000 bottles are affected.
Gas-X Extra Strength simethicone 125 mg softgels are being recalled because of contamination with a diluted propylene glycol-based coolant leaked from a machine during packaging.
Three lots of the Siemens Dimension Tacrolimus Flex reagent cartridge are being recalled because of a potential positive bias in quality control and patient sample results.
Halyard Towel Six Packs, kit code AMTS70-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 224 kits affected.
Hintermann Series Talar Implants, Left, Size 2, are being recalled because packaging and labeling for a left implant contained a right implant device. 67 units are affected.
CORFLO Safety PEG Kits with ENFit Connector, catalog number 50-4320, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 49 kits affected.
Plum Solo Precision IV Pumps are being recalled because under certain conditions the pump may not display a soft limit alert before delivery starts, potentially leading to under- or over-delivery.
Boston Scientific Clik X Anchors, model SC-4318, are being recalled because the sterile anchors may lack sterility assurance. 43 units are affected.
Allia IGS 5 Pulse angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on. 121 units affected.
Halyard Eye Bag Packs, kit code UIEB48-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 60 kits affected.
TDC VELOCE 25G Two Dimensional Cutters are being recalled following an increase in complaints of a loose outer knife, including reports of it loosening during use.
Halyard Drape Packs, kit code LMDP36-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 72 kits affected.
Zep Alcohol Sanitizer Spray, ethanol 70%, in 55-gallon drums is being recalled for microbial contamination. Five drums are affected.
Park St. Deli Macaroni & Cheese, 20 oz, is being recalled because of undeclared soy lecithin. The action covers 58,405 cases.
MIC Safety PEG Kits, 20 Fr PUSH OTW, catalog number 7170-20, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 901 kits affected.
MIC Safety PEG Kits, 24 Fr PUSH OTW, catalog number 7170-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 132 kits affected.