State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Valspar is recalling Cabot wood cleaner and brightener products because faulty cap seals may cause leaks, posing a chemical hazard.
Livin' Lite is recalling 2017 Camplight and Quicksilver RVs because a rubber propane gas line can melt and cause a fire. Dealers will replace the line with a copper extension.
Lippert Components is recalling specific 7000lb and 8000lb Brake Axles because loose flange nuts may cause brakes to lock up or fail to engage, increasing crash risk.
Hospira is recalling specific lots of Fentanyl Citrate Injection ampules because broken tips may compromise sterility.
AtriCure is recalling COBRA Fusion Ablation Systems because a part may separate and remain in the body, potentially causing permanent impairment or damage.
Seth Ellis Chocolatier is recalling Free2b Sun Cups Chocolate due to potential contamination with milk ingredients. The recall covers 189 master cases distributed nationwide.
BioLite is recalling BaseLanterns and BaseLantern XLs because the lithium-ion batteries can overheat and catch fire. One report of minor property damage has been received.
VistaPharm is recalling Lactulose Solution, USP, 10 g/15 mL, because bulk solution tested positive for Burkholderia cepacia bacteria.
Pfizer is voluntarily recalling 2,666 bottles of LEVOXYL (levothyroxine sodium) 200 mcg tablets nationwide because the product is superpotent.
Merit Medical Systems is voluntarily recalling 178 Fluid Management Sets due to a compromised sterile barrier.
Cedar Crest Specialties is recalling Enlightened Peanut Butter Chocolate Chip Ice Cream because some pints may contain undeclared peanuts due to packaging errors.
Merit Medical Systems is recalling 53 Procedure Kits due to a compromised sterile barrier. The kits were distributed nationwide to specific states and Japan.
CSC Motorcycles is recalling 2015-2016 Cyclone motorcycles because they may lack a required label reminding users to use DOT 4 brake fluid.
Hologic is recalling SURESOUND22 uterine sound multipacks because a breach in the sterile barrier compromises product sterility.
EN-R-G Foods is recalling Cherry Lime, Raspberry, and Juneberry Protein Chews due to consumer complaints of nausea and vomiting after consumption.
Merit Medical Systems is recalling 40 Manifold Kits (Catalog No. K09-11867AP) because the sterile barrier is compromised, posing a risk of infection.
Merit Medical Systems is voluntarily recalling 130 MeriTrans Pressure Monitoring Kits because a compromised sterile barrier may affect product sterility.
DePuy Orthopaedics is voluntarily recalling ACTIS Flex Reamers because the instruments may break and leave pieces in patients.
IMUSA is recalling about 17,500 espresso makers because the filler cap can crack or pop off, posing burn and impact risks.
Toshiba American Medical Systems is recalling Aquilion Prime CT systems because cooling oil in the x-ray tube heat exchanger may leak during operation.
Cummins is recalling 164 model year 2015-2016 generator sets because door hinges may fail, causing doors to detach and create road hazards.
Philips is recalling 1,363 CT scanners because the patient support tabletop may fail to move horizontally during scans due to a mechanical linkage failure.
LGS Industries is recalling 2017 Pace, Cargo Express, and Look cargo trailers because a defective weld could cause the ramp door bracket to detach, creating a crushing hazard.
EN-R-G Foods is recalling Cherry Lime Protein Chews due to consumer complaints of nausea and vomiting after consumption.
Merit Medical Systems is voluntarily recalling specific Procedure Kits due to a compromised sterile barrier, which may affect the sterility of the contents.