State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Arrow International Inc is recalling Maximal Barrier Drapes because unsealed packaging may compromise product sterility. The recall affects 416,055 units distributed in the US and 34 other countries.
Arrow International is recalling 416,055 central venous catheterization kits because unsealed packaging may compromise product sterility.
Joerns Healthcare is recalling 915 P.R.O. Matt and ProCair Mattresses because incorrect connectors were supplied, lacking internal shutoff valves required to prevent air loss.
Arrow International is recalling 416,055 central venous catheter kits because unsealed packaging may compromise product sterility.
Joerns Healthcare is recalling specific ProCair and P.R.O. Matt mattresses because they were supplied with connectors lacking required internal shutoff valves, which can cause air to escape from the mattress cells.
Arrow International Inc. is recalling 416,055 Two-Lumen Central Venous Access Kits because unsealed packaging may compromise product sterility.
Arrow International is recalling 416,055 Percutaneous Sheath Introducer Kits because unsealed packaging may compromise product sterility.
NordicNeuroLab AS is recalling 36 licenses of nordicBrainEX version 1.1.2 because a software error can cause fiber tracts to be misaligned when switching between image series with identical resolutions.
Arrow International is recalling Radial Arterial Access Kits because unsealed packaging may compromise sterility. The recall covers 416,055 units distributed in the US and 33 other countries.
Arrow International is recalling 5Fr Catheter Clamps with Fasteners because unsealed packaging may compromise product sterility.
Arrow International is recalling 416,055 echogenic needles because unsealed packaging may compromise product sterility. The recall covers products distributed in the US and 34 other countries.
Arrow International is recalling 416,055 epidural needles because unsealed packaging may compromise product sterility. The recall covers distribution in the US and 35 other countries.
Medline Industries is recalling 2,600 units of sterile needle counters because packaging seal creep may compromise sterility.
Arrow International Inc. is recalling 416,055 ECG adapters because unsealed packaging may compromise product sterility.
Arrow International Inc is recalling 0.2 Micron Flat Epidural Filters because unsealed packaging may compromise product sterility.
Medline Industries is recalling sterile needle counters because packaging seal creep may compromise sterility.
Dynarex Corporation is recalling 15 CGA870 oxygen regulators because the dial has an inaccurate flow rate indicator. The devices were distributed in Massachusetts and New Jersey.
Medline is recalling sterile needle counters because packaging seal creep may compromise sterility. The product is used to count surgical sharps.
Arrow International is recalling 416,055 ARROWg+ard Blue PLUS Pressure Injectable Two-Lumen CVC Kits because unsealed packaging may compromise product sterility.
Arrow International Inc is recalling Radial Artery Catheterization Kits because unsealed packaging may compromise product sterility.
Arrow International is recalling VPS Rhythm ECG Accessory Packs with Johans Adapters because unsealed packaging may compromise product sterility.
Arrow International is recalling specific central venous catheterization kits because unsealed packaging may compromise product sterility.
Continental is recalling specific Coach HA3 tires because visible cords through the innerliner can cause sudden air loss and loss of vehicle control.
Ducati is recalling 2017-2018 Supersport motorcycles because fuel hoses may melt near the exhaust, causing a fuel leak and fire risk.
Manac is recalling 2013-2018 Steel Dropdeck, 2017 Extendable Steel Dropdeck, and 2018 Steel Flatbed trailers because lashing chains may break, allowing cargo to slide or tip.