State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Tearscience is recalling LipiFlow Thermal Pulsation Systems because the labeled storage temperature does not match tested conditions for the full shelf life.
BioMerieux SA is recalling ETEST Imipenem IP32 Foam packaging because the current shelf-life claims are not supported by internal testing.
Vygon MFG is recalling 30,700 AMS-636 Microbore extension sets because the package displays an incorrect priming volume.
BioMerieux SA is recalling ETEST Tobramycin antimicrobial susceptibility testing strips because their shelf-life claims are not supported by internal testing.
BioMerieux SA is recalling ETEST Vancomycin antimicrobial susceptibility testing strips because their shelf-life claims are not supported by internal testing.
BioMerieux SA is recalling Etest Benzyl Penicillin PG256 FOAM packaging because shelf-life claims are not supported by internal testing.
Philips is recalling 11 Brilliance BigBore Oncology CT scanners because retrospective 4D CT scans may display incorrect phase annotations.
BioMerieux SA is recalling ETEST Ciprofloxacin CI 32 Foam products because their shelf-life claims are not supported by internal testing.
AvKARE Inc. is recalling 116 cartons of 500 mg Famciclovir tablets because the product exceeded specifications for unknown impurities.
BioMerieux SA is recalling ETEST Ceftriaxone antimicrobial susceptibility testing strips because their shelf-life claims are not supported by internal testing.
Teleflex Medical is recalling 7,600 units of Green Non-Latex Robertazzi Nasopharyngeal Airways due to a labeling error. The voluntary recall covers products distributed in the US, Canada, and Mexico.
ReVision Optics is recalling 1,279 Raindrop Near Vision Inlays to update instructions for use regarding irrigation and medication timing.
Pfizer is recalling specific lots of Quillivant XR extended-release oral suspension because the product failed to meet dissolution specifications at 12 months.
Pfizer is recalling Quillivant XR extended-release oral suspension due to failed dissolution specifications at 12 months.
Pfizer is recalling Quillivant XR extended-release oral suspension because it failed to meet dissolution specifications at 12 months. The recall affects 28,938 units distributed nationwide.
Schwarze is recalling 2013-2017 street sweepers because incorrect air brake fittings may cause air leaks and unexpected vehicle stops.
Look Cycle is recalling about 800 road bikes and Aerostems because a stainless steel clamp can corrode and break, posing a fall and crash hazard.
Hyundai is recalling 2017 Elantra vehicles because a damaged steering connector may cause loss of power steering assist, increasing crash risk.
SolarWorld is recalling about 97,000 solar panel connectors sold in the U.S. because microscopic cracks can allow moisture to leak in, posing an electrical shock hazard.
Ford is recalling 2017 Edge vehicles with Panoramic Vista Roofs due to an improperly welded windshield header that reduces lateral structural integrity.
Ford is recalling 2017 F-450 and F-550 Superduty trucks because the driveline may vibrate and fracture at highway speeds, potentially causing loss of motive power and increasing crash risk.
Great Dane is recalling 2018 Everest SS refrigerated trailers because a front brake chamber plug may be loose, potentially reducing brake pressure and increasing stopping distance.
Motor Coach Industries is recalling 2014-2016 J4500 vehicles because the front sway bar may crack and detach, increasing crash risk.
Ford is recalling 2013-2015 Escape, Fiesta, Fusion, and Transit Connect vehicles with 1.6L engines because low coolant can cause the engine head to crack, leak oil, and start a fire.
Ford is recalling 2013-2014 Lincoln MKZ, Ford Fusion, and 2014 Ford Fiesta vehicles because door latches may break, leaving doors unsecured.