State
73,809 recalls have nationwide distribution and so reach Massachusetts. 8,252 additional recalls listed Massachusetts specifically in their distribution scope.
Of the 8,252 recalls naming Massachusetts we have scored against our rubric, 1,179 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,360 (29%) are Severe.
Which agencies issued them
These figures cover only the 8,252 recalls whose distribution notice names Massachusetts specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Autocar is recalling 761 2019 Xpeditor vehicles because the power steering assist cylinder bracket may not be properly secured, potentially causing a loss of steering ability.
ARBOC is recalling 2015-2018 Spirit of Freedom, Mobility, and Independence buses because foldaway seat cushions may not stay locked during a crash.
Iowa Mold Tooling Co. is recalling Omnex Proportional Wireless Transmitters because a failing diode may cause cranes to move unexpectedly, increasing injury risk.
PACCAR is recalling 2013-2019 Kenworth and Peterbilt trucks because missing reflex reflectors reduce visibility and increase crash risk.
Thor Motor Coach is recalling 2017-2019 Challenger, Miramar, and Outlaw motorhomes because the driver's windshield roller shade may unroll unexpectedly, blocking visibility.
Honda is recalling 2017-2018 Civic Hatchback and Type R vehicles because the owner's guide may be missing or lack required child restraint information.
Restoration Hardware is recalling specific metal-wrapped coffee tables because the metal tops may contain lead, posing a health risk to children.
Volvo is recalling 2019 VNL and VHD trucks because specific Bridgestone tires may lose air rapidly, increasing crash risk.
Polaris is recalling 2015-2016 Slingshot motorcycles equipped with backup cameras because internal failures can cause fires or disable taillights, increasing crash risk.
Mack is recalling 818 2019 LR, Granite, and TerraPro trucks because specific Bridgestone tires may lose air rapidly, increasing crash risk.
Jennie-O is recalling raw ground turkey products produced in September 2018 due to possible Salmonella Reading contamination linked to a multi-state outbreak.
LÍLLÉbaby is recalling about 6,600 Active Series baby carriers because a sliding chest-clip strap can detach, posing a fall hazard to the child.
Wabash is recalling 2014-2019 Van trailers because limb deflectors may detach while moving, increasing crash risk. Dealers will remove the parts free of charge.
OriGen Biomedical is recalling 134 units of the VV19F Reinforced Dual Lumen Cannula because the extension tube may separate from the hub, posing a risk of blood loss.
Silver Star Brands is recalling Native Remedies VertiFree Oral Spray due to microbial contamination. Consumers should stop using the product and return it to the point of purchase.
Silver Star Brands is recalling Native Remedies EyeClear Pro Oral Spray due to microbial contamination. Consumers should stop using the product and return it to the retailer.
Silver Star Brands is recalling 53 bottles of Native Remedies VaricoGo Oral Spray due to microbial contamination. The product was distributed nationwide in the United States.
Silver Star Brands is recalling 95 bottles of Native Remedies HypoSlim Oral Spray due to microbial contamination. The product was distributed nationwide in the US.
Qualgen, LLC is recalling specific lots of Testosterone 200mg pellets nationwide due to a lack of assurance of sterility.
Qualgen, LLC is recalling Estradiol 10mg pellets nationwide due to a lack of assurance of sterility. The affected lots have specific expiration dates.
Qualgen, LLC is recalling specific lots of Testosterone 87.5mg pellets nationwide due to a lack of assurance of sterility.
Roche Diagnostics is recalling CoaguChek XS Prothrombin Time test strips nationwide because they may produce abnormally high INR results.
Ford is recalling 2019 F-250, F-350, and F-450 Super Duty trucks because an incorrect transmission casting may allow unintended vehicle movement.
Oscor, Inc. is recalling TB Series Bipolar Pacing Leads because the connector cap housing may slide, potentially exposing the connection wire and causing loss of pacing.
Zimmer Biomet is recalling 6,180 units of the RapidFlap SpinDown Clamp because the nut was assembled incorrectly. The device is used to re-attach bone flaps after craniotomy.