State
73,106 recalls have nationwide distribution and so reach New Hampshire. 4,472 additional recalls listed New Hampshire specifically in their distribution scope.
Of the 4,472 recalls naming New Hampshire we have scored against our rubric, 606 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 858 (19%) are Severe.
Which agencies issued them
These figures cover only the 4,472 recalls whose distribution notice names New Hampshire specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
CABTREO acne medication was stored outside refrigeration requirements. The recalled lot was kept at room temperature instead of required refrigerated conditions.
The disk bay component in certain Philips Azurion x-ray systems may fail, potentially preventing diagnostic imaging and delaying procedures. Affected units have been distributed worldwide.
Baxter Healthcare is recalling 13,000 bags of norepinephrine bitartrate injection due to an overwrap label incorrectly showing 4 mg/250 mL concentration, while the primary bag label correctly shows the actual 8 mg/250 mL strength.
Bestco LLC is recalling Meijer Cherry Cough Drops due to potential glass and silicone particulates found during manufacturing quality control inspections. Consumers should stop using the product immediately.
Henry Schein Inc. and Glove Club HSI Gloves Inc. are recalling 1,099 vials of Adrenalin (Epinephrine) Injection because the expiration date on the repack pouch label is incorrect. The product was distributed nationwide.
Bestco LLC is recalling Equate Cherry Cough Drops nationwide due to potential glass and silicone particulates from manufacturing deviations. Affected products are 30-drop and 160-drop bags expiring December 31, 2026.
Abiomed is releasing software Version 8.5 for the Automated Impella Controller to fix an issue in versions 8.4 and 8.4.1 where the device failed to recognize the pump. Approximately 4,463 units were distributed nationwide.
Isuzu is recalling certain FTR, FVR and Chevrolet LCF trucks with Mobileye Collision Warning Systems because a misrouted camera cable can damage wiring and overload the electrical circuit.
Philips Allura Xper fluoroscopic X-ray systems may experience memory module failures that cause the system to stop functioning and prevent imaging. This malfunction could delay critical medical procedures.
Philips is recalling 14 units of its Azurion 3 surgical imaging system due to a potential short circuit in the power inverter. The defect could cause the device to lose power and fail during surgical procedures.
W&H Surgical handpiece S-12 devices were incorrectly laser marked with '1:1' instead of the correct '1:2' during production. 160 units are affected.
Amneal Pharmaceuticals is recalling 46,037 bottles of Oseltamivir Phosphate Oral Suspension due to failed quality test results showing impurities and degradation. The FDA classified this as a Class II recall affecting nationwide distribution.
Meta Psyllium Fiber Capsules in 100 and 160 count bottles are being recalled because the product labeling is illegible. Approximately 21,428 cases were distributed across most US states.
Toyota is recalling certain 2022-2023 Tacoma trucks because the rear axle shaft may separate from the axle housing due to debris causing improperly secured fasteners, increasing the risk of a crash.
Nissan is recalling certain 2023-2024 vehicles, including the Rogue, due to a manufacturing issue that may allow the driver's air bag inflator to absorb moisture and deploy improperly.
Tesla is recalling certain 2013-2022 Model S, X, 3, and Y vehicles because a factory reset can mute the Pedestrian Warning System sounds, increasing crash risk for pedestrians.
USDA FSIS issued a public health alert for Nurture Life Chicken Parm with Super Veggie Spaghetti due to an undeclared egg allergen. Consumers with egg allergies should not consume the product.
Lippert is recalling MTP 20K Surge Brake Couplers with part number 2023050981 because incorrect labels may allow the brake system to be overloaded.
Pierce Manufacturing is recalling 2023-2024 Commercial Chassis because a firmware defect in specific multiplex nodes can cause electrical circuits to overheat and potentially start a fire.
Daimler Coaches is recalling 2022-2024 Mercedes-Benz Tourrider vehicles because the roof hatch handle may break, potentially delaying emergency exits.
LiveWire is recalling certain 2024 S2 Del Mar motorcycles because the Vehicle Supervisory Control software may initiate a powertrain shutdown. 523 units are affected.
Pleasant Valley Teardrop Trailers is recalling 2023-2024 nuCamp truck campers with Lithium Upgrades because an incorrect battery disconnect switch may overheat and cause a fire.
Kia is recalling 2020 Telluride vehicles because high beam headlights may fail, reducing visibility and increasing crash risk.
PACCAR is recalling certain 2009-2024 Kenworth trucks because the air tanks have an insufficient volume of air for the brake system, which can reduce braking performance.
Ford is recalling EcoSport rear seat covers that may prevent air bags from deploying correctly, increasing injury risk in a crash.