State
73,722 recalls have nationwide distribution and so reach Massachusetts. 8,248 additional recalls listed Massachusetts specifically in their distribution scope.
Of the 8,248 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 2,356 (29%) are Severe.
Which agencies issued them
These figures cover only the 8,248 recalls whose distribution notice names Massachusetts specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Teva Pharmaceuticals is recalling Metoclopramide Injection because manufacturing areas exceeded microbial acceptance levels, creating a lack of sterility assurance.
Teva Pharmaceuticals is recalling Desmopressin Acetate Injection because manufacturing areas exceeded microbial limits, compromising sterility assurance.
Teva Pharmaceuticals is recalling Leucovorin Calcium for Injection because manufacturing areas exceeded microbial recovery levels, compromising sterility assurance.
Porsche is recalling certain 2015-2018 Macan models because the front passenger seat occupancy sensor may fail to detect a passenger, preventing the air bag from deploying.
Teva Pharmaceuticals is recalling specific lots of MethyIPREDNISolone Acetate Injectable Suspension because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Hong Thai Foods Corp is recalling Golden Boy Custard Muffin Banana packages due to undeclared milk discovered during New York state sampling.
Teva Pharmaceuticals is recalling specific lots of Vecuronium Bromide for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Teva Pharmaceuticals is recalling Leucovorin Calcium for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Teva Pharmaceuticals is recalling 15,043 vials of MethyIPREDNISolone Acetate Injectable Suspension because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Teva Pharmaceuticals is recalling Epoprostenol Sodium for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Teva Pharmaceuticals is recalling specific lots of Sterile Diluent for Epoprostenol Sodium for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Teva Pharmaceuticals is recalling Toposar (etoposide) injection vials because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Teva Pharmaceuticals is recalling specific lots of MethyIPREDNISolone Acetate Injectable Suspension because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Teva Pharmaceuticals is recalling Epoprostenol Sodium for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Teva Pharmaceuticals is recalling Dacarbazine for Injection USP because manufacturing areas exceeded microbial recovery levels, compromising sterility assurance.
Haro Bicycles is recalling approximately 510 Masi Evoluzione and Gran Corsa bicycles from model years 2017-2020 because the fork steerer tube can break, causing riders to lose control and fall.
Ortho-Clinical Diagnostics is recalling deformed VITROS Chemistry VersaTips that may cause assay results to be biased by up to +/-16%.
Northgate Technologies is recalling 25 ConMed 50L abdominal insufflators because an internal tubing component was made with untested material.
Altec is recalling 2017-2019 DC1317 and DRM12 wood chippers because a flexible exhaust pipe section may separate, creating an exhaust gas leak that increases the risk of a fire.
Natus Manufacturing Limited is recalling 7 units of the EDS 3 CSF External Drainage System because the device failed to meet pyrogen test requirements for endotoxins.
Respironics is recalling 94 Philips V60 ventilator batteries because they were shipped without proper design verification. The recall covers distribution across multiple U.S. states.
Smiths Medical is recalling specific lots of Bivona Cuffless FlexTend Tracheostomy Tubes because they may have been packaged with the wrong neck flange, posing a risk of patient injury.
Nissan is recalling 2016-2019 Sentra vehicles because a contaminated brake light switch may prevent brake lights from illuminating, increasing crash risk.
Covidien is recalling Parietex hydrophilic anatomical mesh where the package label indicates left-side use but contains a right-side device. This labeling error can lead to implant failure and hernia recurrence.
Volkswagen is recalling certain 2021 Atlas and Atlas Cross Sport vehicles due to improperly machined wheel lug bolt holes that may prevent wheels from attaching properly, risking wheel separation and crashes.