State
72,982 recalls have nationwide distribution and so reach Massachusetts. 8,211 additional recalls listed Massachusetts specifically in their distribution scope.
Of the 8,211 recalls naming Massachusetts we have scored against our rubric, 1,171 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,013 (25%) are Severe.
Which agencies issued them
These figures cover only the 8,211 recalls whose distribution notice names Massachusetts specifically. The 72,982 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Eugia US LLC is recalling Gentamicin Injection, USP (Pediatric), 20 mg per 2 mL due to failed color absorbance test results during 12-month stability analysis. The recall affects 48,000 vials distributed nationwide.
Pluslife SARS-CoV-2 Card nucleic acid testing kits were distributed in the U.S. without required FDA premarket authorization. The FDA is recalling approximately 1,850 boxes distributed nationwide and internationally.
Guangzhou Pluslife Biotech is recalling the MiniDock Integrated Nucleic Acid Testing Device (Model PM001) because it was distributed in the U.S. without required FDA premarket authorization.
Aurobindo Pharma USA Inc is recalling Amazon Basic Care Acetaminophen 325 mg tablets due to confirmed consumer complaints of brown surface discoloration on tablets, a cGMP deviation.
Hangzhou AcoSound Technology Co., Ltd. is recalling 120 units of the AcoSound Model LW12-BTE-M hearing aid due to labeling errors, including incorrect manufacturer attribution, missing manufacturer business address, and incomplete UDI information.
GEM is recalling 2022-2025 e2, e4, e6, and eLXD vehicles because improperly tightened fasteners may cause the front lower ball joint to separate, potentially leading to a loss of steering control.
Mack is recalling 2024-2026 MD Electric trucks because the engine may fail to return to idle if communications are interrupted, increasing crash risk.
Keystone RV Company is recalling 2025 Fuzion and Raptor toy haulers because reversed generator fuel hoses may increase fire risk.
Keystone is recalling 2025 Carbon, Fuzion, and Raptor toy haulers because missing rear gate pins or leg support brackets may allow the gate to shift, increasing injury risk.
Kawasaki is recalling 2025 W230 ABS motorcycles because an unstable electrical ground connection may cause the engine to stall, increasing crash risk.
Daimler Trucks is recalling certain 2020-2026 Western Star 49X and 2021-2026 47X vehicles because a stud connecting the battery to the starter at the frame rail may have been incorrectly installed.
Forest River is recalling certain 2025-2026 Wildwood and Salem travel trailers because the exterior transit latch on the rear patio door cannot be unlocked from inside the vehicle.
Forest River is recalling 2026 Sabre fifth wheel recreational trailers because the exterior griddle may be incorrectly installed, allowing it to be stowed while still connected to LPG, increasing fire risk.
Kia is recalling 2020-2022 Niro EV vehicles because a damaged rearview camera circuit board may prevent the image from displaying, increasing crash risk.
Forest River is recalling certain 2026 Spirit travel trailers because the installed safety chains may not meet the actual Gross Vehicle Weight Rating, posing a risk of trailer separation from the tow vehicle.
Vanguard is recalling 2021-2023 VXP 28-Foot Pup trailers because the pintle hook box assembly may crack or break, reducing stability while being towed.
Subaru is recalling certain 2025 Forester vehicles because the child seat anchor bolts may have been improperly tightened, allowing them to come loose.
Honda is recalling 2013 Accord vehicles with 4-cylinder engines and CVTs in 23 states and D.C. because the driveshaft may corrode and break, potentially causing a loss of drive power or vehicle rollaway.
Supreme is recalling 2025 Wabash trucks because insufficient lubrication on the liftgate pin may cause it to seize, leading to liftgate failure and injury risk.
Shyft Group is recalling 2024-2025 Utilimaster Aeromaster vehicles because the 360-degree camera monitor may not display the correct image at startup, increasing crash risk.
Mazda is recalling certain CX-50 Hybrid and CX-50 vehicles because incorrectly configured module software may cause the airbag to deploy improperly. All affected vehicles are under dealer control.
Amneal Pharmaceuticals is recalling Sulfamethoxazole and Trimethoprim Tablets (400 mg/80 mg) nationwide due to microbial contamination that may cause black spots on tablets. The contamination affects non-sterile products distributed across the USA.
Philips is recalling three Intera 1.5T Achieva Nova-Dual MRI systems worldwide due to a gradient coil component failure that can generate smoke and fire, posing risks including burn injury and asphyxia.
Sysco Corporation is recalling Created Fresh Sub-Tuna Salad on Everything Ficelle (5.76 oz.) due to potential Salmonella contamination from cucumbers used in the product.
Lipman Family Farms is recalling 24-count repacked cucumbers distributed across 18 states due to potential Salmonella contamination. Consumers should not consume the product and should discard or return affected cucumbers.