State
73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur aTG test kits due to positive bias in anti-thyroglobulin results compared to WHO standards.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur aTG test kits due to positive bias in anti-thyroglobulin results compared to WHO standards.
PerkinElmer is recalling AutoDELFIA hCG Kits because hCG concentrations may be decreased by 15-20% at the lower measuring range.
Bard Medical Division is recalling specific lots of ArcticGel Pads because the hydrogel may not adhere properly to the pad.
US Worldmeds LLC is recalling 6,456 vials of Revonto (dantrolene sodium for injection) because the reconstituted solution showed out-of-specification precipitate during stability testing.
Siemens Medical Solutions is recalling 53 SOMATOM Definition Edge CT scanners due to a software issue that may cause scans to abort in Dual Spiral Dual Energy mode.
Lin-Zhi International Inc is recalling 49 Ethyl Alcohol Enzymatic Assay kits due to potential detergent contamination that may reduce shelf life.
Advantice Health is recalling Dermoplast Anesthetic Spray canisters because some full cases contain cans labeled with an incorrect net weight of 2.75 oz instead of 2.0 oz.
Advantice Health is recalling Dermoplast Anesthetic Spray canisters because the label incorrectly states the net weight as 2.75 oz instead of 2.0 oz.
Hercules Enterprises is recalling 2018 CH40GN 18047 trailers because improperly installed wheel end nut locking devices may allow wheels to separate from the axle.
Aero Industries is recalling Easy Cover tarping systems because a spring return pin may not be welded, allowing the pawl assembly to separate and increase crash risk.
Conagra Brands is recalling P.F. Chang's Home Menu Chicken Pad Thai and Chicken Fried Rice products because they contain undeclared milk, a known allergen.
Tyson Foods is recalling approximately 11.8 million pounds of frozen chicken strips that may contain pieces of metal. The recall follows consumer complaints of foreign matter and oral injuries.
Supreme is recalling 2018-2019 Platform vehicles because the rear clearance lamp may be positioned incorrectly, blocking required light spread and increasing crash risk.
Taylor Made Ambulances is recalling 2017-2018 Ford and GMC-based ambulances because Whelen brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.
Motor Coach Industries is recalling specific 2018-2019 MCI buses because temperature and vibration stresses may cause the tempered glass roof hatch to shatter, potentially injuring passengers.
BRP is recalling approximately 10,000 2017 Ski-Doo MXZ, Summit, and Renegade snowmobiles because a fuel leak can cause a fire. No injuries have been reported.
Greenfield World Trade is recalling Excalibur EZ DRY food dehydrators because they can overheat, posing a fire hazard and causing minor burn injuries.
Suzuki is recalling 2010-2013 Kizashi vehicles because the front passenger air bag may deactivate if the system misclassifies an adult as a child.
FIRMAN Power Equipment is recalling P03615 portable generators sold at Costco because the carbon canister can leak gas, posing a fire hazard.
Yamaha is recalling 198 2019 YZFR3 motorcycles because porosities in the front brake lever may cause it to break under strong force, increasing crash risk.
Edwards Lifesciences is recalling Fogarty Dilation Atrioseptostomy Catheters due to reports of balloon fragmentation or detachment and difficulty deflating the balloon after deployment.
Edwards Lifesciences is recalling Miller Balloon Atrioseptostomy Catheters due to difficulty deflating the balloon and reports of fragmentation or detachment.
COVIDIEN LLC is recalling 7,248 units of the Endo Clinch II Auto Suture Grasper because the sterilization method used was not consistent with the labeling and approved method.
Guangzhou Improve Medical Instruments is recalling 550,000 Prevent G Safety Winged Blood Collection Sets because the hub needle detached during use.