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.
A-S Medication Solutions LLC is recalling Valsartan Tablets 160 MG because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Philips is recalling SureSigns VS4 monitors because lithium-ion batteries may overheat or ignite if not replaced on time, posing injury and property damage risks.
Philips is recalling SureSigns VS3 monitors because lithium-ion batteries may overheat or ignite if not replaced on time, posing fire and injury risks.
Siemens is recalling 3D V ceiling stands because the primary load-bearing rope could break, causing the arm to drop and potentially seriously injuring patients or users.
Thor Motor Coach is recalling 2018-2019 Outlaw 29J motorhomes because improper 12V wiring may increase the risk of fire during an electrical short circuit.
Nature's Bounty is recalling specific lots of Blue Green Algae supplements because a high level of microcystin was observed in the product.
Country Favor Inc. is recalling Best Taste Brand Sliced Ginger because it contains high levels of undeclared sulfites. The product was distributed to retail stores in 18 states.
A-S Medication Solutions LLC is recalling 178 bottles of Valsartan Tablets, 80 MG, because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Hetero Labs Limited is recalling Valsartan tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Hetero Labs is recalling Valsartan tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Handicare USA Inc. is recalling four P600 Series patient lifts due to premature strap wear and breakage at maximum weight conditions.
Philips is recalling DigitalDiagnost Rel.4 Upgrades because a defective hook may allow the footplate to fall or swing, potentially injuring patients or operators.
Entegra Coach is recalling 2018 Odyssey vehicles because damaged leveling system hydraulic hoses may leak fluid onto the exhaust system, increasing the risk of a fire.
Philips is recalling DigitalDiagnost Release 3 units because a defective hook may allow the footplate to fall or swing, posing a risk of injury to patients or operators.
Hetero Labs Limited is recalling Valsartan tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Hetero Labs Limited is recalling Valsartan tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Compass Health Brands is recalling CPAP mask cushions because a design change makes them incompatible with previous elbow parts, potentially causing unacceptable CO2 porting.
Banks Square Market Corp is recalling summer squash noodles due to potential Listeria monocytogenes contamination. The product was distributed in Massachusetts, Maryland, and New York.
Philips is recalling two DigitalDiagnost 4 Flex units because a defective hook allows the footplate to fall, posing an injury risk to patients or operators.
Philips is recalling DigitalDiagnost Release 3 units because a defective hook may allow the footplate to fall or swing, posing an injury risk to patients or operators.
Dole Fresh Vegetables is recalling a limited quantity of Classic Coleslaw due to the potential for metal fragments in the product.
Philips is recalling DigitalDiagnost 4 Flex and Value units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Philips is recalling CombiDiagnost R90 units because a defective hook may allow the footplate to fall, posing an injury risk to patients or operators.
Philips is recalling DigitalDiagnost 4 Chest units because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Becton Dickinson is recalling BD BBL GC-Lect Agar plates because some were made with Gentamicin instead of Vancomycin, which may cause false negative gonorrhea test results.