State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Unilever is recalling Ben & Jerry's Brownie Batter Core Ice Cream because certain pints may contain soft plastic pieces.
Midwest International Corp is recalling dried vegetable products because they are acidified foods without a registered manufacturer or scheduled process.
Stanmore Implants Worldwide Ltd. is recalling 15 femoral stem components because customer inquiries reported that the device stem punctured the packaging pouch.
Stryker Howmedica Osteonics Corp. is recalling specific lots of GAM Kirschner Wires and T2 K-Wires because a manufacturing error may have compromised the sterile pouch seal.
Brownwood Farms is recalling Jalapeno Cherry Salsa because it contains Yellow 5, an ingredient not declared on the label.
Stanmore Implants Worldwide Ltd. is recalling 51 tibial components because the device stem may have punctured the sterile packaging.
Teleflex Medical is recalling Flexi Nozzle Long sprayers because they may produce a straight stream instead of an atomized plume, potentially causing inadequate anesthesia.
Amendia, Inc. is recalling Savannah-T Straight Rods because some packages have unacceptable seals with compromised integrity.
Stryker is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because they may exhibit signs of corrosion.
Synthes (USA) Products LLC is recalling 31 units of the VA Implant Rack for the Compact Distal Radius System because incorrect assembly could cause screws to touch the surface beneath the rack.
Ortho-Clinical Diagnostics is recalling VITROS CRP Slides because the diluent contains endogenous CRP, which can cause falsely high test results if not subtracted.
Zydus Pharmaceuticals is recalling Bupropion Hydrochloride Extended-Release Tablets because they failed to meet dissolution specifications at the 6-month time point.
PerkinElmer is recalling 73 EnLite Neonatal TREC Kits because the Unique Device Identifier (UDI) is missing from the outer box labels.
Les Emballages Knowlton Inc. is recalling Tom's of Maine Naturally Dry Natural Powder Antiperspirant Stick because an incorrect back label was applied to the product.
Amendia, Inc. is recalling 5,833 units of K-Wires because the packaging seals are unacceptable, with some showing compromised integrity due to channels or voids.
Kalmar is recalling 1,639 Ottawa T2 vehicles because an unprotected chassis power board may allow moisture to cause an electrical short and fire.
Southwest is recalling 2013-2016 QP25, QP35, and QP45/50 trailer-mounted generators because the trailer tongue may separate, creating a road hazard.
Daimler Vans USA is recalling 2017 Mercedes-Benz Metris vans because the front passenger air bag may not vent properly in a crash, increasing injury risk.
Honda is recalling 2016 Odyssey vehicles because the second row center seat may slide unexpectedly. This defect increases the risk of injury in a crash.
Honda is recalling 2011-2016 Odyssey vehicles because the second row outboard seat release lever may remain unlocked, allowing the seat to move unexpectedly during a crash.
HME is recalling 2015-2016 Type-6 Wildland trucks because the certification label may list an incorrect Gross Vehicle Weight Rating, potentially leading to vehicle overload.
Gillig is recalling 451 CNG transit buses because gas detection electronics may fail to warn operators of system malfunctions, increasing fire risk.
Gold Medal Packing is recalling approximately 4,607 pounds of boneless veal products due to possible E. coli O26 and O45 contamination. No illnesses have been reported.
DRV Suites is recalling 2016-2017 Elite and Mobile Suites fifth wheel trailers because brake caliper bolts may loosen, potentially causing a loss of braking capability.
Mack is recalling certain 2012-2017 trucks because front wheel hubs may fail, potentially causing loss of vehicle control or dropped parts.