State
73,806 recalls have nationwide distribution and so reach New Hampshire. 4,483 additional recalls listed New Hampshire specifically in their distribution scope.
Of the 4,483 recalls naming New Hampshire we have scored against our rubric, 603 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,049 (23%) are Severe.
Which agencies issued them
These figures cover only the 4,483 recalls whose distribution notice names New Hampshire specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Eldorado is recalling 2012-2018 Goshen shuttle buses because a wheelchair lift cam may fail, allowing the platform to rise too high and risk injury.
Oshkosh is recalling 2014-2019 S-Series Glider vehicles because incorrectly placed strobe lights may confuse other drivers and increase crash risk.
Ford is recalling 2019 Fusion Energi Hybrid vehicles because they may not adequately protect against high voltage contact during normal operation.
New Flyer is recalling 172 transit buses because the rooftop emergency escape hatch glass may shatter in extreme cold, posing an injury risk to passengers.
Toyota is recalling 2019 Camry Hybrid and Avalon Hybrid vehicles because the fuel filler pipe may not be properly connected, posing a fire risk.
Ferrari is recalling 2,150 vehicles because a cracked fuel vapor separator may leak fuel, increasing the risk of fire.
PurpleAir is recalling PowerStream power supply units for air sensors because they can overheat, posing fire and burn hazards. No injuries have been reported, but 27 reports of sparks or smoke were received.
CVB is recalling LUCID Folding Mattress-Sofas because they fail to meet the mandatory federal flammability standard for mattresses, posing a fire hazard.
Ferrari is recalling 2017-2019 GTC4Lusso and 2018-2019 GTC4Lusso T vehicles because tension on the door lock mechanism may prevent doors from opening with the external handle.
Smiths Medical is recalling Portex 550 ml Sterile Water Humidifiers because leaking containers may compromise sterility, potentially exposing patients to infectious agents.
Smiths Medical is recalling Portex 350 ml Sterile Water Humidifiers because leaking containers may expose patients to infectious agents.
Funky Chunky LLC is recalling Nutty Choco Pop because the label fails to declare that the product contains cashews and almonds.
Smiths Medical is recalling Portex 550 ml Sterile Water Humidifiers because leaking containers may compromise sterility, potentially exposing patients to infectious agents.
Medex Cardio-Pulmonary Inc. is recalling 54,924 Medline Prefilled 550 ml Sterile bags due to leaking containers that may compromise sterility.
Terrific Care LLC is recalling CoaguChek XS PT Test Strips sold via MedEx Supply due to potential for abnormally high INR test results.
Smiths Medical is recalling Portex 1000 ml Sterile Water USP Pour Bottles because leaking containers may lack sterility assurance, posing a risk of exposure to infectious agents.
Smiths Medical is recalling Portex Unit Dose 5 ml Normal Saline because leaking containers may lack sterility assurance, posing a risk of exposure to infectious agents.
Smiths Medical is recalling 106,000 units of Portex 5ml Normal Saline due to leaking containers that may compromise sterility and expose patients to infectious agents.
Smiths Medical is recalling Medline sterile water humidifiers because leaking containers may expose patients to infectious agents.
Medex Cardio-Pulmonary Inc. is recalling 235,560 units of Medline Prefilled 350 ml Sterile Solution because leaking containers may compromise sterility and expose patients to infectious agents.
Smiths Medical is recalling Intermed 550 ml Sterile Water Humidifiers due to leaking containers that may compromise sterility and expose patients to infectious agents.
Smiths Medical is recalling Portex Unit Dose 15 ml Normal Saline products because leaking containers may compromise sterility, potentially exposing patients to infectious agents.
Dana Incorporated is recalling certain Ultimate Dana 44 Front Axles because the pinion tail bearing may seize, preventing the axle from rotating and increasing crash risk.
Smiths Medical is recalling Intermed 350 ml Sterile Water Humidifiers due to leaking containers that may compromise sterility and expose patients to infectious agents.
Smiths Medical is recalling Portex 500 ml Sterile Water USP Pour Bottles because leaking containers may compromise sterility and expose users to infectious agents.