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.
ICU Medical is expanding a recall of I.V. Administration Sets with NanoClave manifolds due to potential leaks or separation between the female luer and the manifold.
Merit Medical Systems is recalling specific lots of Flex-Neck Classic Peritoneal Dialysis Catheters (Pediatric) due to a mix-up with adult catheters.
Confidence Inc. is recalling Prenatal Multi-V + DHA tablets because they contain undeclared ingredients, including HPMC and several food dyes.
Terumo is recalling 128 CDI System 500 monitors because a subset of devices fail the automated H/Sat Color Chip Test. This failure disables the H/Sat module but does not cause device inaccuracy.
Arrow International Inc. is recalling 7,024 units of Hands-Off Multi-Lumen Central Venous Catheters because packaging may not be sealed, potentially compromising sterility.
Severino Pasta Manufacturing is recalling Cheese Raviolini because the bottom label incorrectly identifies the product as Rigatoni and omits eggs, creating an allergen mislabeling risk.
Terumo is recalling 128 CDI Blood Parameter Monitoring System 500 H/SAT units because a hybrid intensity shift causes the automated Color Chip Test to fail, disabling the H/Sat module.
Confidence Inc. is recalling Nitro-Cross 60s supplements due to undeclared ingredients including HPMC and Titanium Dioxide.
Siemens Medical Solutions USA is recalling 605 ARTIS Pheno interventional fluoroscopic X-ray systems due to a potential hardware issue that may cause thermal effects and damage to system parts.
Dr. Reddy's is recalling 40 mg Atorvastatin Calcium tablets because stability testing showed impurity levels exceeding specifications.
Merit Medical Systems is recalling 22,234 units of 1mL Medallion Syringes due to a manufacturing defect in the plunger tip.
Nico Corp. is recalling 204 sterile Shepherd's Hook accessories because they were shipped with incorrect transport labels instead of product labels.
Orexigen Therapeutics is recalling 95,296 bottles of Contrave extended-release tablets due to customer complaints of punctures in the bottles.
Richard-Allan Scientific is recalling 1,039 cases of EZ Single Cytofunnel Brown units due to mislabeling. The recall is voluntary and nationwide.
Prana Biovegan Inc. is recalling Organic Dried Figs because the product may contain insects. The recall affects specific lots distributed to Pennsylvania and Massachusetts.
Confidence Inc. is recalling Glucosamine Plus tablets because they contain undeclared ingredients, including Hydroxypropyl Methylcellulose and Titanium Dioxide.
Clarity Diagnostics is recalling specific lots of Clarity 10SG Urinalysis Strips because they lack a Canister Code Bar Code Label, making them incompatible with Clarity Urocheck 120 Urine Analyzers.
Confidence Inc. is recalling Glucosamine Plus tablets because they contain undeclared ingredients, including Hydroxypropyl Methylcellulose and Titanium Dioxide.
Tosoh Bioscience is recalling 9 AIA Analyte Application Manual CDs due to unapproved product labeling. The CDs were distributed to six US states.
Forest River is recalling 2014-2019 recreational trailers because a wiring defect may prevent brakes from engaging if the trailer detaches from the tow vehicle.
Confer Plastics is recalling Curve in-pool step systems because children's limbs can become entrapped in side openings, posing a drowning risk.
Nissan is recalling 2017-2018 models including the Versa, Sentra, and NV200 because the ignition switch may shift, causing the engine to stall and increasing crash risk.
Ford is recalling 2018-2019 Edge, Flex, MKX, and MKT vehicles because improperly secured power supply cables may cause an electrical arc, increasing the risk of a fire.
Volkswagen is recalling 2018 Atlas vehicles because a twisted air conditioning drain tube may allow water to enter the air bag control module, potentially causing unintentional air bag deployment.
Allison is recalling certain H 50 and H 40 Drive Units because pressure switches may fail, causing a loss of drive and increasing crash risk.