State
72,992 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 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Head Rush Technologies is recalling approximately 410 TRUBLUE auto belay devices sold online from May 2023 through December 2024 because they can fail to retract, posing a fall hazard. One incident resulted in a fractured leg.
REV Recreation Group is recalling certain 2022-2025 Fleetwood and Holiday Rambler motorhomes because the engine exhaust tip may detach, allowing exhaust fumes to enter the cabin.
Volkswagen is recalling certain 2021-2023 ID.4 and 2022-2023 Audi Q4 e-Tron vehicles because the instrument panel may not properly display the transmission gear lever indicator, failing FMVSS 102.
Canyon Bicycles USA recalls about 1,400 Speedmax CF triathlon bicycles due to fork steerer tubes that can crack or break, creating a fall hazard. The company is offering free repairs at authorized service centers.
Wayfair recalls about 1,555 Style Life Eleven baby loungers due to suffocation, fall, and entrapment hazards that violate federal infant sleep safety standards. Stop using them and contact Wayfair for a refund.
Orange EV is recalling 2023-2024 HUSK-E XP terminal trucks because the rear weight rating placard is incorrect and tires may be inadequate, increasing crash risk.
P.J. Salvage recalled approximately 9,400 children's pajama sets and robes sold at Nordstrom Rack because they violate federal flammability regulations, posing a risk of burn injuries to children. No injuries have been reported.
Costway is recalling about 4,400 Babyjoy high chairs due to suffocation and entrapment hazards. The chairs were designed or marketed for infant sleep with excessive incline and have unsafe gaps where children can become trapped.
Kichler Lighting has recalled approximately 2,760 Ellerbeck Wall Sconces because electrical wires can become damaged at the adjustable joints, creating a risk of electric shock. No injuries have been reported.
Forever 21 recalled about 24,700 children's pajamas sold nationwide from November 2023 through November 2024 due to flammability violations. The pajamas don't meet federal safety standards for children's sleepwear and pose a burn injury risk.
ARVA Neo BT Pro Avalanche Transceivers with defective fuses may lose battery power during use, preventing emergency transmission in avalanche rescues. About 1,067 units sold between September 2022 and January 2025 are affected.
Philips is recalling the Allura Xper FD10C patient examination table due to a mattress defect that may allow patients to fall from the table. The device was distributed worldwide.
Spectranetics' Intact Vascular Tack Endovascular System may fail to deploy properly or migrate in blood vessels, potentially causing ischemia and requiring additional intervention.
Philips recalls Allura Xper FD20 fluoroscopy patient tables due to a mattress issue that may cause patients to fall during procedures.
Paras Premium Golden Raisins are being recalled due to undeclared sulfites (56.8mg per serving), which can cause serious allergic reactions in sensitive individuals.
Philips recalls Azurion 7 M20 patient tables due to a mattress defect that could cause patients to fall. Approximately 1,480 units in the US and 2,741 units overseas are affected.
Philips is recalling Azurion 5 M20 imaging tables worldwide due to a mattress defect that could cause patients to fall from the table. This FDA Class I recall involves 632 units.
Philips Medical Systems is recalling Azurion 7 B12 examination tables due to a mattress-related patient fall risk. The recall affects 602 total units, including 94 in the US and 508 internationally.
Philips Medical Systems is recalling the Allura Xper FD20 Biplane OR Table due to a mattress defect that could cause patients to fall during surgery. 3 units are affected globally.
Philips is recalling Allura Xper FD10 imaging devices because the patient table mattress may not securely hold patients during procedures, creating a fall hazard. The recall affects 2,274 units worldwide, including 459 in the U.S.
Provepharm Inc. is recalling Phenylephrine HCl Injection vials (Lot 24020027) due to the presence of particulate matter. The affected medication was distributed nationwide.
Alvogen has recalled Fentanyl Transdermal System patches (25 mcg/h) nationwide due to a manufacturing defect where patches may be stacked together in a single pouch. Patients using affected lots should contact their healthcare provider.
Philips is recalling Azurion 3 M12 patient tables due to possibility of patient falling from the table related to the mattress. The recall affects 263 units distributed in the US and internationally.
Philips Allura Xper FD20 Biplane x-ray tables are being recalled due to a mattress defect that could cause patients to fall. The recall affects 479 units distributed worldwide.
Philips recalls Azurion 3 M15 imaging tables due to mattress defects that could cause patients to fall from the examination table.