The Recall Desk

State

New Jersey product recalls

72,820 recalls have nationwide distribution and so reach New Jersey. 9,751 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total
9,751
Critical
1,249
Severe
2,480
Most recent
2026-09-09

Of the 9,751 recalls naming New Jersey we have scored against our rubric, 1,249 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,480 (25%) are Severe.

These figures cover only the 9,751 recalls whose distribution notice names New Jersey specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

626–650 of 82571

  • SevereCPSC·26636·2026-07-23

    Sviyatp Pool Drain Covers Recalled for Entrapment and Drowning Risk

    About 670 Sviyatp pool drain covers sold online violate federal safety standards and pose entrapment and drowning hazards. Consumers should stop using affected pools immediately and contact Sviyatp for a refund.

    Product
    Sviyatp Pool Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V478000·2026-07-23

    BMW S 1000 RR Motorcycles Recalled Due to Potential Engine Stall Risk

    BMW is recalling certain 2020-2026 S 1000 RR motorcycles because vibration may cause ignition lock failure, leading to engine stalls or electrical system failures.

    Product
    BMW — BMW S 1000 RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26634·2026-07-23

    12-Drawer Fabric Dressers Recalled for Tip-Over and Entrapment Hazards

    Romorgniz 12-Drawer Fabric Dressers sold on Amazon pose tip-over and entrapment risks to children if not anchored to the wall. About 10,040 units are affected.

    Product
    Romorgniz 12-Drawer Fabric Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26633·2026-07-23

    EnHomee 9-Drawer Fabric Dressers Recalled for Tip-Over and Entrapment Hazard

    EnHomee 9-Drawer Fabric Dressers sold on Walmart.com pose a risk of serious injury or death from tip-over and entrapment if not anchored to the wall. About 16,809 units are affected.

    Product
    EnHomee 9-Drawer Fabric Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E048000·2026-07-23

    K&N and Spectre Fuel Filters Recalled for O-Ring Disintegration

    K&N Engineering is recalling specific K&N and Spectre replacement fuel filters because the O-ring may disintegrate, causing leaks or clogs.

    Product
    FUEL SYSTEM, OTHER:FUEL FILTER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26639·2026-07-23

    Personalized Baby Bibs and Stroller Bags Recalled for Choking Hazard

    Peony Design has recalled personalized baby bibs and stroller bags sold online because snaps can detach, posing a choking risk to young children. The company is offering refunds.

    Product
    Personalized Baby Bibs and Stroller Bags
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26635·2026-07-23

    Sili Factory Pull String Teething Toys recalled for choking hazard risk

    Aojieni Silicone is recalling about 5,918 Sili Factory Pull String Teething Toys because the silicone strings violate toy safety standards and can lodge in a child's throat, posing a serious choking risk.

    Product
    Sili Factory Pull String Teething Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26637·2026-07-23

    OeyUoc Pool Drain Covers Recalled for Entrapment and Drowning Hazards

    OeyUoc white pool drain covers sold on Amazon violate safety standards and pose entrapment and drowning risks. About 404 units have been recalled; consumers should stop using them immediately.

    Product
    OeyUoc Pool Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V476000·2026-07-23

    Forest River Recalls 2027 Travel Trailers with Incorrect Water Tank Labels

    Forest River is recalling 2027 travel trailers because the Federal Placard may list an incorrect fresh water tank capacity, which could lead to vehicle overloading.

    Product
    FOREST RIVER — FOREST RIVER UNMAPPED, SURVEYOR, IBEX, NO BOUNDARIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2682-2026·2026-07-22

    ABIOMED Impella CP Heart Pump Introducer Sheath Leakage Risk

    Abiomed is recalling the Impella CP heart pump set (87,277 units worldwide) due to potential leakage from the introducer sheath that cannot be visually detected by users. The defect affects the 14Fr and 23Fr introducers included in every pump set.

    Product
    ABIOMED Impella CP Set, Pump Set Code 0048-0003, containing BIOMED Impella Introducer, 14 Fr, 13 cm & 25 cm, Product Code 0052-3046. heart pump and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1171-2026·2026-07-22

    D'Dioses Mango Ice Pops Recalled for Undeclared Allergens

    D'Dioses Mango Ice Pops (3.7 oz) are being recalled because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. Consumers with allergies or sensitivities to these ingredients should not consume the product.

    Product
    Ice Pop, D'Dioses Mango, 3.7 oz (81.7 g), with UPC 827912008494
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-2689-2026·2026-07-22

    ABIOMED Impella CP Heart Pump Set Introducer Sheath Leakage Risk

    ABIOMED is recalling Impella CP heart pump sets worldwide due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines in 14Fr and 23Fr introducers. The manufacturing defect is not visually detectable.

    Product
    ABIOMED Impella CP Set, Pump Set Code 0048-0014; containing Introducer Product Code 0052-3046. heart pump and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1170-2026·2026-07-22

    D'Dioses Grocella Ice Pop Recalled for Undeclared Allergens

    D'Dioses Fruit Pops, Inc. is recalling D'Dioses Grocella Ice Pop (1 bar, 81.7 g) due to undeclared milk, pecans, pistachios, yellow #5, and red #40. The product was distributed in NJ, CT, NY, and PA.

    Product
    Ice Pop, D'Dioses Grocella, 1 Bar (81.7 g), with UPC 827912008531
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-2690-2026·2026-07-22

    Abiomed Impella CP Smart Assist Set Heart Pump Introducer Sheath Leakage

    Abiomed is recalling the Impella CP Smart Assist Set due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines in 14Fr and 23Fr introducers. These manufacturing issues are not visually detectable.

    Product
    ABIOMED Impella CP Smart Assist Set, JP, Pump Set Code 0048-0024-JP; containing Introducer Product Code 0052-3025-JP. heart pump and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1159-2026·2026-07-22

    D'Dioses Fresa Leche Ice Pop Recalled for Undeclared Allergens

    D'Dioses Fresa Leche ice pops may contain undeclared milk, pecans, pistachios, and food colorings (yellow #5 and red #40). The product was distributed in NJ, CT, NY, and PA.

    Product
    Ice Pop, D'Dioses Fresa Leche, 4 oz (85 g), with UPC 710594511850
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0689-2026·2026-07-22

    Cleviprex Injectable Emulsion Recall Due to Sterility Assurance Concerns

    Chiesi USA, Inc. is recalling Cleviprex (clevidipine) injectable emulsion due to lack of assurance of sterility. The affected product is distributed nationwide.

    Product
    CLEVIPREX — CLEVIPREX (CLEVIPIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1173-2026·2026-07-22

    Ice Pop D'Dioses Nanche Recalled for Undeclared Allergens

    D'Dioses Fruit Pops, Inc. is recalling D'Dioses Nanche ice pops because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. The product was distributed in NJ, CT, NY, and PA.

    Product
    Ice Pop, D'Dioses Nanche, 1 Bar (81.7 g), with UPC 827912008449
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-2709-2026·2026-07-22

    Bone Marrow Tray kits recalled due to sterility failure

    Argon Medical Devices is recalling Bone Marrow Tray kits containing Lidocaine HCL Injection because they do not meet sterility release criteria.

    Product
    Bone Marrow Tray, REF: CB0033TL; CB0355TLA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1163-2026·2026-07-22

    Ice Pop D'Dioses Vainilla Recalled for Undeclared Allergens

    D'Dioses Fruit Pops, Inc. is recalling D'Dioses Vainilla ice pops because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. The products were distributed in NJ, CT, NY, and PA.

    Product
    Ice Pop, D'Dioses Vainilla, 4 oz (85 g), with UPC 710594511829
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-2687-2026·2026-07-22

    ABIOMED Impella 5.5 Heart Pump Introducer Sheath Leakage Risk Recall

    Abiomed is recalling the Impella 5.5 Smart Assist Set heart pump due to potential leakage from introducer sheaths. The defect is not visually detectable and affects all affected pump sets worldwide.

    Product
    ABIOMED Impella 5.5 Smart Assist Set, JP, Pump Set Codes 1000211, 1000212; containing Introducer Product Code 0052-3006-JP. heart pump and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2688-2026·2026-07-22

    Abiomed Impella 5.5 SmartAssist S2 heart pump introducer sheath leakage risk

    Abiomed is recalling Impella 5.5 SmartAssist S2 heart pump sets worldwide due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines that may not be visible to users.

    Product
    ABIOMED Impella 5.5 SmartAssist S2 Set, JP, Pump Set Codes 1000459, 1000460; containing Introducer Product Code 0052-3006-JP. heart pump and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2684-2026·2026-07-22

    ABIOMED Introducer Kit 23 Fr heart pump accessory leakage risk

    Abiomed is recalling ABIOMED Introducer Kit 23 Fr due to potential sheath leakage from manufacturing defects. The leakage risk is not visually detectable and affects all current batches worldwide.

    Product
    ABIOMED Introducer Kit 23 Fr, 11 cm, Pump Set Code 1000441, containing Kit, 23Fr Introducer, 11cm, Sterile, Introducer Product Code 2000342. heart pump and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide