The Recall Desk

State

New York product recalls

73,584 recalls have nationwide distribution and so reach New York. 12,947 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total
12,947
Critical
1,511
Severe
3,698
Most recent
2026-10-21

Of the 12,947 recalls naming New York we have scored against our rubric, 1,511 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,698 (29%) are Severe.

These figures cover only the 12,947 recalls whose distribution notice names New York specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1–25 of 86531

  • CriticalCPSC·27051·2026-10-29

    NTI and HTP Gas Boilers Recalled for Fire and Carbon Monoxide Risks

    Ariston is recalling NTI and HTP residential gas boilers because a cracked condensate dish can cause fire, carbon monoxide poisoning, or impact injuries.

    Product
    NTI and HTP residential gas boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·27060·2026-10-29

    Harkla Recalls Children's Sensory Swings Due to Fall Hazard

    Harkla is recalling children's sensory swings because the ceiling hook can separate from its plate, posing a risk of serious injury from a fall.

    Product
    Harkla Sensory Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·27054·2026-10-29

    DREO Recalls DR-HSH015 Space Heaters Due to Fire and Burn Hazards

    DREO is recalling DR-HSH015 space heaters because they can overheat and ignite, posing fire and burn hazards. Consumers should stop using the heaters immediately.

    Product
    DREO Space Heaters, model DR-HSH015
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·27061·2026-10-29

    Pamag Pieeoo Mattresses Recalled for Fire Hazard Risk

    Longjili Trading is recalling Pamag Pieeoo mattresses because they violate mandatory flammability standards, posing a risk of serious injury or death from fire.

    Product
    Pamag Pieeoo Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·27047·2026-10-29

    PILLANI Recalls Nursing Pillows Due to Suffocation Risk

    PILLANI is recalling nursing pillows that violate safety standards and pose a risk of infant suffocation. Consumers should stop using them immediately and request a refund.

    Product
    PILLANI Nursing Pillows
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·27058·2026-10-29

    RootStim Recalls Minoxidil Hair Treatment Bottles Due to Child Poisoning Risk

    RootStim is recalling three minoxidil hair regrowth products because the bottles lack required child-resistant packaging, posing a poisoning risk to young children.

    Product
    RootStim 5% Minoxidil Foam Hair Regrowth Treatment with Rosemary and Biotin, RootStim Minoxidil Hair Regrowth Treatment 5% Minoxidil Rosemary & Biotin and RootStim Minoxidil Hair Regrowth Treatment 5% Minoxidil with Rosemary
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·27045·2026-10-29

    QZH.DUAO Children's Pajama Sets Recalled for Burn Hazard

    QZH.DUAO children's pajama sets are being recalled because they violate mandatory safety standards, posing a risk of serious burn injuries.

    Product
    QZH.DUAO Children’s Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·27038·2026-10-22

    CPSC Recalls CIYTI Light-Up Princess Costumes Due to Battery Ingestion Risk

    The CPSC is recalling CIYTI Light-Up Princess Costumes because accessible button batteries pose a risk of serious injury or death if swallowed. Consumers should stop using the costumes and contact the seller for a refund.

    Product
    CIYTI Light-Up Princess Costumes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·27039·2026-10-22

    VQQQ Gas Patio Heaters Recalled for Fire and Burn Hazards

    VQQQ natural gas patio heaters are being recalled because malfunctioning components can release gas, posing a risk of serious injury or death from fire and burns.

    Product
    VQQQ Natural Gas Patio Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·27041·2026-10-22

    Lithonia Lighting Recalls RSX Luminaires with Adjustable Tilt Arms

    Lithonia Lighting is recalling RSX luminaires with specific adjustable tilt arm mountings because the knuckle can fail, causing the fixture to fall and pose a risk of serious injury.

    Product
    Lithonia Lighting RSX Luminaires with AASP, AARP, AAWB, and AAWSC Adjustable Tilt Arm Mountings used for commercial outdoor lighting.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V701000·2026-10-22

    Chrysler Recalls 2026 Dodge Durango for Tail Light Wiring Harness Defect

    Chrysler is recalling 2026 Dodge Durango vehicles because damaged tail light wiring harness terminals may cause the lights to fail, reducing visibility and increasing crash risk.

    Product
    DODGE — 2026 DODGE DURANGO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E076000·2026-10-22

    Chrysler Recalls MOPAR Tail Lights Due to Wiring Harness Damage

    Chrysler is recalling specific MOPAR tail lights because damaged wiring harness terminals may cause the lights to fail, reducing vehicle visibility.

    Product
    EXTERIOR LIGHTING:TAIL LIGHTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0001-2027·2026-10-21

    Instrumentation Laboratory Recalls HemoslL AcuStar HIT-lgG In Vitro Diagnostic

    Instrumentation Laboratory is recalling 434 units of the HemoslL AcuStar HIT-lgG in vitro diagnostic due to potential for invalid calibration curves or negative mean bias of up to 47% with patient samples.

    Product
    HemoslL AcuStar HIT-lgG(PF-4). Part Number: 0009800127. in vitro diagnostic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0146-2027·2026-10-21

    SI-BONE iFuse TORQ Implant System Recalled for Sterility Assurance Issues

    SI-BONE, Inc. is recalling 100 units of iFuse TORQ Implant System screws because packaging seal integrity testing failed, preventing assurance of sterility.

    Product
    iFuse TORQ Implant System Model/Catalog Number: 10055T(10x55mm), 10060T(10x60mm), 10065T(10x65mm), 10080T(10x55mm), 11580T(11.5x80mm)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0136-2027·2026-10-21

    JenaValve Trilogy Delivery Catheter Recalled for Sleeve Liner Separation

    Jenavalve Technology Inc. is recalling 143 JenaValve Trilogy Delivery Catheters due to a defect that may prevent heart valve deployment.

    Product
    JenaValve Trilogy Delivery Catheter, Size 27MM REF: TRILOGY-DC-L
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0160-2027·2026-10-21

    Beckman Coulter DxU 840m and 850m Iris Recalled for Check Valve Defect

    Beckman Coulter is recalling DxU 840m and 850m Iris analyzers because a check valve defect can cause fluid leaks, creating slip, chemical, and biohazard risks.

    Product
    DxU 840m Iris, REF: C76947; DxU 850m Iris, REF: C49513
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V700000·2026-10-21

    PACCAR Recalls Kenworth and Peterbilt Trucks for Fuel Hose Separation Risk

    PACCAR is recalling specific Kenworth and Peterbilt trucks because remote fuel filter hoses may separate, causing fuel leaks, engine stalls, and increased fire or crash risks.

    Product
    KENWORTH — KENWORTH, PETERBILT T380, 548, T480, 567
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0137-2027·2026-10-21

    Medtronic Recalls Grafton DBM Allografts Due to Donor Microbial Presence

    Medtronic is recalling 18 units of Grafton DBM and Grafton Plus DBM products because the donor tissue tested positive for Clostridium butyricum, posing a potential infection risk.

    Product
    Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined with an inert additive to yield a demineralized bone matrix (DBM) allograft product having a particular physical form and/or handling property. Grafton DBM Gel and Grafton Plus DBM Paste are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0153-2027·2026-10-21

    Ethicon Recalls Silk Surgical Sutures Packaged with Alcohol-Based Fluid

    Ethicon is recalling 1,764 units of PERMA-HAND Silk sutures that were packaged with alcohol-based fluid. The fluid is not part of the product design and could cause surgical delays or treatment failure if used.

    Product
    PERMA-HAND Silk Black Braided Sterile Nonabsorbable Surgical Suture, 1X18" TF-5, Product Code: N271H
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0039-2027·2026-10-21

    Zydus Recalls Hydrocortisone Sodium Succinate Injection for Impurity Failures

    Zydus Pharmaceuticals is recalling 70,776 vials of Hydrocortisone Sodium Succinate for Injection due to failed impurities and degradation specifications.

    Product
    HYDROCORTISONE SODIUM SUCCINATE — HYDROCORTISONE SODIUM SUCCINATE (HYDROCORTISONE SODIUM SUCCINATE)
    Category
    Drug
    Distribution
    Distributed nationwide