State
73,827 recalls have nationwide distribution and so reach New Jersey. 9,782 additional recalls listed New Jersey specifically in their distribution scope.
Of the 9,782 recalls naming New Jersey we have scored against our rubric, 1,246 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,944 (30%) are Severe.
Which agencies issued them
These figures cover only the 9,782 recalls whose distribution notice names New Jersey specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Suzuki is recalling 2017-2018 GSX-R1000 motorcycles because a gear shift error can cause the drive chain to break, leading to power loss and crash risk.
Wayfarer is recalling 2017 24 QW recreational vehicles because the installed Kidde fire extinguishers may clog or detach, potentially failing to function during a fire.
Forest River is recalling 2018 Cherokee recreational trailers because side marker lights are improperly positioned and reflectors may be missing, reducing visibility.
Newmar is recalling 2018 Essex motorhomes because low beam headlights do not illuminate when high beams are activated, reducing driver visibility.
Aston Martin is recalling 2017-2018 DB11 V12 and V8 Coupe vehicles because the driver's frontal air bag may deploy unexpectedly due to insufficient grounding.
Newmar is recalling 2017-2018 Ventana and Dutch Star motorhomes because low beam headlights do not illuminate with high beams, reducing visibility.
KZRV is recalling 2017-2018 Durango Gold recreational trailers because the rear sofa may block the exit window handle, increasing injury risk in emergencies.
Panasonic is recalling 55-inch flat screen televisions with tabletop swivel stands because the mounting screws can loosen, causing the TV to tip over and potentially injure or kill children.
Café Spice GCT Inc. is recalling ready-to-eat chicken salad products because they contain milk, an undeclared allergen, and are mislabeled as chicken wraps.
Multipro Baby Cradle N Swings are being recalled because they fail to meet federal safety standards, posing fall and entrapment hazards to babies.
Bed Bath & Beyond is recalling UGG Hudson comforters due to a risk of mold exposure. Consumers should stop using the products and return them for a full refund.
Hillsdale Furniture is recalling Polston and Collin bar stools because the seat can loosen or break off, posing a fall hazard. No injuries have been reported.
Nodine's Smokehouse Inc. is recalling smoked salmon packages nationwide due to potential Listeria monocytogenes contamination.
Teva Pharmaceuticals is recalling specific bottles of Moexipril Hydrochloride and Hydrochlorothiazide tablets because routine stability testing found high levels of a degradation impurity.
Daisy's Bakery Inc. is recalling Gourmet Concha products because they contain an undeclared milk allergen. The mislabeled items were distributed to five states.
CareFusion is recalling Alaris Syringe Pump Model 8110 units because the syringe plunger grippers may fail to close automatically, potentially affecting medication delivery.
Cordis Corporation is recalling 511 units of the S.M.A.R.T. Flex Biliary Stent System due to a potential for cracked luer hubs.
Harrisburg Dairies is recalling 365 brand and Harrisburg Dairies brand Egg Nog because dried egg yolks were not listed in the ingredient statement.
Lovebiotics, LLC is recalling The Coconut Cult Mango Cream Probiotic Coconut Yogurt because the allergen statement lists sodium caseinate but fails to identify milk as the source.
Orthoscan is recalling Mobile Mini C-arm systems because a software defect allows users to activate Digital Zoom during live imaging, exposing a larger x-ray field than is visible to the user.
American Sugar Refining is recalling bulk sugar syrup distributed in the U.S. after customers found fine metallic powder and steel wool strands in the product.
Orthoscan is recalling 2,012 Mobile Mini C-arm systems because a software defect allows users to activate Digital Zoom during live imaging, exposing a larger x-ray field than is visible to the user.
King Systems Corp. dba Ambu, Inc. is recalling 871,116 Universal Flex2 Breathing Circuits due to potential leak test failures.
OrthoScan is recalling 2,012 Mobile Mini C-arm systems because a software defect allows users to activate Digital Zoom during live imaging, exposing a larger x-ray field than visible.
Repro-Med Systems is recalling HIgH-Flo Subcutaneous Safety Needle Sets because gaps were found in the sterile barrier packaging during post-sterilization inspection.