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.
Bausch & Lomb is recalling Stellaris Elite Vit Cutters because the back cap may separate from the cutter body.
Boston Scientific is recalling VALITUDE X4 CRT-P pacemakers because hydrogen-induced accelerated battery depletion may require early replacement.
Philips is recalling 5,115 Allura Xper F020 DR Tables because the ceiling monitor suspension may detach, posing a risk of injury from falling equipment.
Reckitt Benckiser is recalling Durex Real Feel Polyisoprene Condoms because they failed to meet the required burst pressure specification.
Philips is recalling 5,115 Allura Xper F020 Biplane DR Tables because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Philips is recalling 5,115 Allura Xper FD2O Biplane systems because the monitor ceiling suspension may detach, causing the monitor to fall and risk injury.
Philips is recalling INTEGRIS Allura 15-12 biplane systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Philips is recalling 5,115 medical monitor ceiling suspensions because the monitor may detach and fall, posing an injury risk to patients and users.
Intuitive Surgical is recalling specific da Vinci Surgical System power supply units that were manufactured incorrectly and may fail during use.
Bausch & Lomb is recalling Stellaris Elite vit cutters because the back cap may separate from the body. The defect poses a risk of harm during use.
Philips is recalling INTEGRIS Allura 9 biplane systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Stryker GmbH is recalling 233 units of Hoffmann LRF Hexapod Software because it may compute erroneously accelerated correction plans under specific settings.
Boehringer Ingelheim is recalling 998 bottles of SYNJARDY tablets due to cross-contamination with other products.
Bausch & Lomb is recalling Stellaris Elite 23 GA Vit Cutters because the back cap may separate from the cutter body.
Terumo is recalling 10 Advanced Perfusion System units due to improperly torqued screws on the Power Manager Board, which may cause electrical shorts.
Philips is recalling Allura Xper FD2O systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Philips is recalling 5,115 Allura Xper F020 DR Tables because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Walmart is recalling Ozark Trail camp axes because the axe head can detach from the handle, posing an injury hazard.
Spartan Motors is recalling 2001-2019 MetroStar and Gladiator emergency vehicles because EMS cabinet fasteners may be the wrong size, posing a crash injury risk.
Philips is recalling INTEGRIS Allura 9 F FDXD systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Bausch + Lomb is recalling Stellaris Elite 23 GA Vit Cutters because the back cap may separate from the cutter body.
Philips is recalling 5,115 Allura Xper FD2O Biplane systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Philips is recalling INTEGRIS Allura 15-12 systems because the monitor ceiling suspension may detach, causing the monitor to fall and potentially injure patients, users, or bystanders.
Hetero Labs Limited is recalling 98,016 bottles of Montelukast Sodium 10 mg tablets because a pharmacist reported blue specks on the tablets.
Zimmer Biomet is recalling 16 Vanguard 360 Revision Knee System tibial block augments because the sterile packages contained one bolt instead of the required two.