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.
Synthes (USA) Products LLC is recalling 260 sterile 2.5 mm TI Calibrated Reaming Rods because their peel pouches are delaminating.
West-Ward Pharmaceuticals is recalling specific lots of Phenobarbital Tablets because they failed to meet dissolution specifications at the 12-month stability time point.
Infiniti Creations, LLC is voluntarily recalling HCG ASAP drops due to misbranding and potential undeclared HCG content.
Infiniti Creations, LLC is voluntarily recalling Simeons Program HCG Drops due to misbranding and potential undeclared HCG content.
Pentax of America is recalling video colonoscopes shipped between April 2014 and September 2015 because they included outdated instruction manuals and lacked required reprocessing adaptors.
Infiniti Creations is voluntarily recalling HCG Drops due to misbranding and potential undeclared HCG content.
Merit Medical Systems is voluntarily recalling 107,341 Fluid Administration Sets due to a molding defect in the drip chamber.
Synthes (USA) Products LLC is recalling 319 sterile 3.0 mm Guide Rods because their peel pouches are delaminating.
Zydus Pharmaceuticals USA Inc. is recalling BUPROPION Hydrochloride Extended-Release Tablets, 300 mg, because the product failed to meet dissolution specifications at an intermediate time point.
Infiniti Creations, LLC is voluntarily recalling A New You HCG Drops due to misbranding and potential undeclared HCG content.
Synthes (USA) Products LLC is recalling 139 units of 2.5 mm Guide Rods because their sterile peel pouches are delaminating.
Infiniti Creations, LLC is voluntarily recalling SkinEHCG HCG Drops due to misbranding and potential undeclared HCG content.
Infiniti Creations, LLC is voluntarily recalling Original HCG Drops due to misbranding and potential undeclared HCG content.
Infiniti Creations, LLC is voluntarily recalling HCG Plus drops due to misbranding and potential undeclared HCG content.
Sun Pharmaceutical Industries is recalling KENALOG (Triamcinolone Acetonide) Spray due to low alcohol content. The product failed stability specifications.
Synthes (USA) Products LLC is recalling 1,951 sterile 2.5 mm reaming rods because their peel pouches are delaminating.
Mylan Pharmaceuticals is recalling Diltiazem HCl Extended-Release Capsules because of out-of-specification results for a known compound.
Synthes (USA) Products LLC is recalling 5,478 sterile 3.0 mm reaming rods because their peel pouches are delaminating.
West-Ward Pharmaceuticals is recalling 32,102 bottles of Amoxicillin oral suspension because some bottles are missing the color-coded panel that displays the product strength.
Infiniti Creations, LLC is voluntarily recalling Supervision Weightloss HCG Drops due to misbranding and potential undeclared HCG content.
Van Hool is recalling specific motorcoaches because front steering knuckle carriers may crack, potentially causing a wheel to separate and increasing crash risk.
Gree Electric Appliances is recalling approximately 2.5 million dehumidifiers sold under various brands because they can overheat and catch fire, posing serious fire and burn hazards.
Stanley is recalling about 70,000 commercial door locksets because the latches can fail, preventing doors from being unlocked from the inside during an emergency.
Toyota is recalling 2011-2016 Sienna minivans because the power sliding door may open unexpectedly while the vehicle is moving, increasing the risk of injury to occupants.
Forest River is recalling 2016-2017 StarTrans PS2 buses because the instrument cluster may display 'PARK' instead of 'BRAKE' during a brake malfunction, increasing crash risk.