State
20,371 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.
Forest River is recalling certain 2023 Wildwood, Salem, and Stealth EVO travel trailers. The 8-gauge refrigerator wire lacks over-current protection, creating a fire risk from melted wiring.
Prevost is recalling 2022-2024 H3-45 VIP motorcoaches and 2024 H3-45 models because an incorrect bumper trim panel obstructs the radar sensor, preventing the driver assist system from functioning properly and increasing the risk of crashes.
Jayco is recalling 2023 Solstice and Entegra Expanse recreational vehicles because the HVAC system's defrost and defog controls may stop working. This loss of visibility control increases the risk of crashes under certain driving conditions.
Daimler Vans USA is recalling Freightliner and Mercedes-Benz Sprinter vans from 2021-2023 due to insufficient paint adhesion that may cause windows and interior lashing rails to detach during a crash. No injuries have been reported.
MI Windows and Doors is recalling about 25,000 model 1620 vinyl single-hung impact windows with window opening control devices due to a defective tilt latch that can cause the control devices to malfunction, posing fall and serious injury hazards.
LG is recalling about 52,000 of its 86-inch smart televisions with stands because the stand can become unstable, creating tip-over and entrapment hazards that can result in injuries or death. Consumers should immediately detach the stands and place the TVs in a safe location away from children.
American Honda is expanding its recall of 2019-2021 Honda Talon 1000 recreational off-highway vehicles because a loose intake funnel band screw can enter the engine, cause sudden failure, and result in loss of control and crashes.
Cranberry Sweets & More Inc is recalling Peanut Butter Meltaway chocolates mislabeled as Mint Meltaways. The product contains undeclared peanut, a major food allergen, posing risk to allergic consumers.
Biomerieux is recalling VITEK 2 AST-XN09 test kits where performance cannot be guaranteed due to storage outside proper temperature and time parameters. Affected kits nationwide should not be used.
Biomerieux is recalling one batch of Nephrocheck Liquid Control Reagent because the product was stored outside proper temperature and time parameters, making performance unreliable.
Biomerieux Inc is recalling VITEK 2 Reagent AST-GN73 test kits nationwide because they were stored outside proper temperature and time ranges, potentially compromising test accuracy.
Biomerieux Inc is recalling API 20 E 25 Strips (Batch 1009226560) because temperature and time excursions during storage exceeded specified parameters. Product performance cannot be guaranteed.
Steris Corporation is recalling 338 boxes of VERIFY Dual Species Biological Indicators (Lot #230613) because some units fail to promote spore growth as intended, risking false-negative sterilization test results.
Biomerieux Inc is recalling 7 units of ETEST Clinical Vancomycin VA 256 test kits due to storage temperature excursions that may compromise test performance. Affected kits were distributed nationwide.
Biomerieux Inc. is recalling VITEK 2 Antibiotic Susceptibility Test Kits (AST-GP67) due to storage temperature and time conditions exceeding acceptable limits, which cannot guarantee product performance.
Randox Liquid Assayed Specific Protein Control Level 2 has lost potency in rheumatoid factor, causing laboratory quality control tests to fail and delaying patient test results.
Biomerieux Inc recalled ETEST antibiotic susceptibility test kits from batch 1009384490 due to storage conditions exceeding safe temperature and time parameters, potentially affecting test accuracy.
Siemens is updating software in 638 Programmable Diagnostic Computers distributed in the US to fix four software errors that could crash the device or corrupt password storage, potentially delaying diagnostics.
Biomerieux Inc. is recalling VITEK 2 REAGENT AST-GN69 test kits nationwide due to temperature and time excursions during storage that may compromise product performance.
Biomerieux Inc is recalling PPM Clinical Chromid Candida diagnostic plates because storage temperature and time parameters were exceeded, preventing performance guarantees.
Biomerieux is recalling VITEK 2 AST-GN70 test kits nationwide due to temperature and time excursions that may compromise test performance and diagnostic reliability.
Altimate Medical is recalling the ActiveAid 922 Shower/Commode Chair because a manufacturing defect prevents the frame from folding properly and being secured by the frame strap in the folded position.
Pine Pharmaceuticals is recalling Epi-Caine intraocular injection (11,453 vials nationwide) due to discoloration in raw material used for compounding, a manufacturing quality control failure.
Biomerieux Inc. is recalling VITEK 2 REAGENT GP TEST KIT units nationwide due to temperature and time parameters exceeding acceptable ranges, which may affect test performance.
Biomerieux Inc. is recalling the VITEK 2 REAGENT AST-N801 TEST KIT nationwide due to storage conditions exceeding acceptable ranges, which cannot guarantee product performance.