State
20,096 recalls have nationwide distribution and so reach New Jersey. 0 additional recalls listed New Jersey specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect New Jersey consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
PACCAR is recalling 2025 Kenworth and Peterbilt trucks due to improperly heat-treated ball studs in steering assemblies that may break, causing loss of steering control.
Anker is recalling about 69,000 Soundcore and PowerConf Bluetooth speakers sold on Amazon in 2023 due to overheating lithium-ion batteries. The firm received 33 reports of incidents, including fires and one minor burn injury.
NetZero USA is recalling about 13,000 High Bay LED light fixtures due to plastic pin degradation that can cause the LED board to come loose and catch fire. Seven burning incidents have been reported with no injuries.
Belkin is recalling about 4,000 BoostCharge Pro wireless charger power banks due to a fire hazard from overheating lithium-ion batteries. One unit caught fire and damaged a house.
Winnebago and Itasca recall certain 2020-2023 motorhomes due to improperly tightened seat belt attachments that may fail to restrain occupants in a crash. Dealers will tighten fasteners free of charge.
Vacation Inc. recalls about 13,000 units of Black Label Scented Candles due to flame overheat causing glass breakage and creating fire and laceration risks. No injuries have been reported, but consumers should stop using the product immediately.
Polaris recalled about 2,500 Model Year 2024 Ranger and Bobcat vehicles with a defective passenger side seat belt anchor weld. Consumers should immediately stop carrying passengers and contact an authorized dealer for free repair.
QVC is recalling about 1.1 million pairs of Temp-tations oven gloves that can fail to protect from heat, causing a burn hazard. The company received 162 reports of insufficient protection, including 92 reports of minor burns.
Polaris is recalling about 21,000 RZR XP 1000 and XP 4 1000 recreational off-road vehicles because the battery terminal cover can be damaged by the seat base, exposing the battery post and creating a fire hazard. No injuries have been reported.
Academy Sports + Outdoors is recalling about 6,100 Redfield 12- and 18-gun fireproof safes because mechanical locking plates can fail, potentially allowing unauthorized access. No injuries have been reported.
Forest River is recalling approximately 137 2022 Columbus fifth wheel vehicles because the riser tube between the axle hangers was not installed. This creates inadequate tire clearance, risking tire puncture and vehicle crashes.
Hologic has recalled 12,710 BioZorb Markers nationwide after receiving reports of serious complications including infection, device migration, and device erosion. The FDA classified this as a Class I recall.
MEDLINE epidural trays used for labor anesthesia may have connectors that fail to fully open, preventing proper catheter insertion. The recall affects 2,592 units distributed across the US and internationally.
Treehouse Foods recalls Duncan Hines griddle waffle mix due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and best-by dates from October 2024 to October 2025.
Philips is recalling 5,231 SENSE Breast Coils due to a potential patient safety hazard during scan preparation and performance. The FDA has not disclosed specific details about the nature of the risk.
Absorbine Jr. Ultra Strength Pain Patch is being recalled nationwide due to manufacturing process deviations. The voluntary recall affects approximately 4,968,000 patches.
GE Medical Systems is recalling three SIGNA Architect AIR MRI systems due to gradient coils that can produce elevated acoustic noise during scanning. The units were distributed to the US and 12 countries worldwide.
Multiple brands of frozen mini griddle waffles manufactured by Treehouse Foods are being recalled due to potential Listeria monocytogenes contamination affecting approximately 9.9 million cases nationwide.
Multiple brands of frozen blueberry waffles manufactured by Treehouse Foods are recalled due to potential Listeria monocytogenes contamination. Approximately 9.9 million cases were distributed nationwide in the USA and Canada.
Medline Industries is recalling 408 surgical kits from Alabama, Georgia, Massachusetts, New Jersey, and Pennsylvania. Some suture packages within the kits contain incorrect needle types and sizes, and incorrect suture diameters and lengths.
Treehouse Foods is recalling frozen griddle pancakes from Wegmans, Yelloh, and Giant Eagle brands due to potential Listeria monocytogenes contamination. The products were distributed nationwide across the USA and Canada.
Treehouse Foods is recalling Duncan Hines, Bakers Source, and Gordon Choice branded griddle waffles due to potential Listeria monocytogenes contamination. Products were distributed nationwide in the USA and Canada.
Treehouse Foods is recalling Good & Gather and Breakfast Best griddle waffles nationwide due to potential Listeria monocytogenes contamination. Affected batches have codes starting with 2C with best-by dates between October 1, 2024 and October 11, 2025.
Treehouse Foods is recalling BREAKFAST BEST plant-based waffles nationwide due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and best-by dates from October 2024 through October 2025.
Medline is recalling 360 surgical implant and thoracotomy kits because some suture packages contain incorrect needle types, sizes, or suture diameters and lengths. The affected kits were distributed to healthcare facilities in five states.