The Recall Desk

State

New York product recalls

73,190 recalls have nationwide distribution and so reach New York. 12,939 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total
12,939
Critical
1,511
Severe
3,148
Most recent
2026-09-30

Of the 12,939 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 3,148 (24%) are Severe.

These figures cover only the 12,939 recalls whose distribution notice names New York specifically. The 73,190 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

13901–13925 of 86129

  • HighCPSC·24738·2024-02-22

    Magik & Kover Pack and Play Mattresses Recalled for Suffocation Hazard

    Magik & Kover Pack and Play Mattresses sold on Amazon are being recalled because they violate federal safety regulations for crib mattresses and pose a suffocation hazard to infants. Consumers should immediately stop using the mattresses and contact the company for a refund.

    Product
    Magik & Kover Pack and Play Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24126·2024-02-22

    Cascade Designs MSR Camping Cooking Pots Recalled for Burn and Scald Hazards

    Cascade Designs is recalling select MSR camping cooking pots because the handle can detach or become loose, spilling hot food and liquids and causing burn or scald injuries. The company has received 22 reports of handle problems, including two burn injuries.

    Product
    MSR camping cooking pots
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24125·2024-02-22

    IKEA ÅSKSTORM 40W USB Chargers Recalled for Burn and Electric Shock Risk

    IKEA is recalling about 22,600 ÅSKSTORM 40W USB Chargers because the cable can become damaged or break over time, creating burn and electric shock hazards. Consumers should stop using the chargers immediately and return them to any IKEA store for a full refund.

    Product
    ÅSKSTORM 40W USB Chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24739·2024-02-22

    Spring Spirit and Biloban Pack and Play Mattresses Recalled for Suffocation Hazard

    The CPSC has recalled Spring Spirit and Biloban pack and play mattresses sold on Amazon.com due to a suffocation hazard to infants. The mattresses violate federal safety regulations and lack required warnings and labels.

    Product
    Spring Spirit and Biloban Pack and Play Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V134000·2024-02-22

    Jaguar I-Pace turn signal flash rate does not warn of failure

    Jaguar is recalling certain 2021-2024 I-Pace vehicles because the turn signal flash rate will not change to warn the driver that a turn signal has stopped working, failing FMVSS 108.

    Product
    JAGUAR — JAGUAR I-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V133000·2024-02-22

    Chevrolet Colorado and GMC Canyon may brake automatically without an obstacle

    GM is recalling certain 2023 Chevrolet Colorado and GMC Canyon vehicles because the front camera module may falsely detect an obstacle and engage automatic emergency braking unexpectedly.

    Product
    CHEVROLET — CHEVROLET, GMC COLORADO, CANYON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24740·2024-02-22

    Polaris MATRYX Snowmobiles Recalled for Primary Clutch Failure Hazard

    Polaris is recalling Model Year 2022–2024 MATRYX snowmobiles with PATRIOT 650 and 850 engines because the primary clutch can fail and separate from the vehicle, creating an injury hazard. Polaris has received 109 reports of clutch failure, including one incident resulting in a laceration injury.

    Product
    Model Year 2022-2024 MATRYX Snowmobiles equipped with PATRIOT 650 and 850 Engines
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V130000·2024-02-22

    Jeep Grand Cherokee high beams may not activate quickly in AUTO

    Chrysler is recalling certain 2023-2024 Jeep Grand Cherokee and Grand Cherokee L vehicles because the driver may be unable to quickly activate the high beams in AUTO, failing FMVSS 108.

    Product
    JEEP — JEEP GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0866-2024·2024-02-21

    Utz Wavy Originals Potato Chips recalled for undeclared milk allergen

    Utz Wavy Originals Potato Chips (2.75 oz) distributed in New York may contain undeclared milk and could pose a risk to people with milk allergies.

    Product
    Utz Wavy Originals Potato Chips, Net WT. 2.75 oz (78g), UPC 0-41780-19014-7.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0903-2024·2024-02-21

    Mexican Style Quinoa Salad Recalled for Undeclared Soy and Egg Allergens

    Hans Kissle Company is recalling Mexican Style Quinoa Salad due to undeclared soy and egg allergens. The product was distributed in the Northeast and may pose serious risk to consumers with allergies.

    Product
    MEXICAN STYLE QUINOA SALAD
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0865-2024·2024-02-21

    Dragonfly Jelly Bar Handbags and Backpacks Recalled for Choking Hazard

    U.S. Tov, Inc. is recalling Dragonfly Jelly Bar Handbags and Backpacks due to a potential choking hazard from konjac. The products were distributed nationwide.

    Product
    Dragonfly Jelly Bar Handbag 11.64oz, 17.63oz UPC Code 721557357156, 721557357163 Dragonfly Jelly Bar Backpack 7.93oz, 28.22oz UPC Code 721557357170, 721557357187
    Category
    Food
    Distribution
    38 states
  • SevereFDA (Devices)·Z-0980-2024·2024-02-21

    Impella Cardiac Support Catheters: Risk of Left Ventricle Perforation

    Impella cardiac catheters are being recalled due to risk of left ventricle perforation during operator use. The FDA has classified this Class I recall affecting 91,914 units worldwide.

    Product
    Impella catheters - Intravascular micro axial blood pumps that support a patient's circulatory system. (1) Product Code 005042 - Impella 2.5 (2) Product Code 005062 - Impella 5.0 (3) Product Code 005082- Impella LD (7) Product Codes 0550-0008 and 1000100 - Impella 5.5…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0874-2024·2024-02-21

    Mighty Fine Chocolate Ice Cream Recalled for Undeclared Peanuts

    Byrne Dairy, Inc is recalling Mighty Fine Chocolate Ice Cream because it contains undeclared peanuts. Consumers with peanut allergies should not consume this product.

    Product
    Mighty Fine Chocolate Ice Cream
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·24V124000·2024-02-21

    Lexus and Toyota Mirai rearview camera images may not display promptly

    Toyota is recalling certain Lexus and Toyota Mirai vehicles with a Panoramic View Monitor because the rearview camera image may not display immediately after shifting into reverse.

    Product
    TOYOTA — TOYOTA, LEXUS MIRAI, LC HYBRID, ES HYBRID, LC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1140-2024·2024-02-21

    FilmArray GI diagnostic kits recalled due to false positive Norovirus results

    BioFire Diagnostics is recalling FilmArray GI diagnostic test kits due to potential signals of increased false positive Norovirus results. Approximately 64,594 kits representing 2.3 million tests have been distributed worldwide.

    Product
    FilmArray Gastrointestinal (GI) Panel RFIT-ASY-0116 (30 test kit) RFIT-ASY-0104 (6 test kit) Gastrointestinal microorganism multiplex nucleic acid-based assay. In vitro diagnostic.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V128000·2024-02-21

    Toyota Camry second-row head restraint brackets may be insufficiently welded

    Toyota is recalling certain 2023-2024 Camry and Camry Hybrid vehicles because second-row head restraint brackets may be insufficiently welded, failing FMVSS 202. 4,212 units affected.

    Product
    TOYOTA — TOYOTA CAMRY, CAMRY HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V125000·2024-02-21

    Toyota Tundra and Lexus LX may move unexpectedly in neutral

    Toyota is recalling certain 2022-2024 Tundra, Tundra Hybrid, Lexus LX600 and 2023-2024 Sequoia Hybrid vehicles because unexpected vehicle movement may occur in neutral without the brakes applied.

    Product
    TOYOTA — TOYOTA, LEXUS TUNDRA HYBRID, SEQUOIA HYBRID, TUNDRA, LX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1087-2024·2024-02-21

    Philips CombiDiagnost R90 Fluoroscopy Device May Display Wrong Patient Images

    The Philips CombiDiagnost R90 fluoroscopy device may display a previous patient's radiography images during an examination, risking privacy violation and diagnostic errors in 86 affected units.

    Product
    CombiDiagnost R90 1.0 (709030)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1141-2024·2024-02-21

    HeartSine Samaritan PAD Defibrillators Recalled for Test Configuration Flaw

    HeartSine samaritan PAD defibrillators shipped in test configuration may have incorrect CPR timing and delayed or no therapy delivery in cardiac events. Users should stop using affected units and contact the manufacturer.

    Product
    HeartSine samaritan PAD (Public Access Defibrillator): Type/Catalog: SAM 350P/350-UNIT-US-10, 350-STR-US-10, 350-STR-UK-10; SAM 360P/360-STR-JA-10, 360-STR-DE-10, 360-STR-UK-10; SAM 450P/450-UNIT-US-08, ; SAM 500P/500-BAS-UK-10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V127000·2024-02-21

    Pierce Recalls 2020-2023 Vehicles Due to Rear Bumper Obstruction

    Pierce Manufacturing is recalling specific 2020-2023 Velocity, Enforcer, and Saber vehicles because a rear bumper option may obstruct rear lights, increasing crash risk.

    Product
    PIERCE — PIERCE ENFORCER, SABER, VELOCITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1076-2024·2024-02-21

    FDA Recalls Heart-Lung Machine Component Over Sterile Barrier Defect

    Maquet is recalling an HLS Set Advanced 5.0 component used in CARDIOHELP heart-lung machines due to a compromised sterile barrier that may cause infection. The recall affects 6,657 US units.

    Product
    Model No. BEQ-HLS 5050 USA, HLS Set Advanced 5.0, Product Code/Part Number 70106.9077. Used with the CARDIOHELP heart-lung machine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1071-2024·2024-02-21

    Olympus Duodenovideoscope Distal Cover may detach during gastrointestinal procedures

    Olympus Single Use Distal Cover MAJ-2315 may detach from duodenovideoscopes during gastrointestinal procedures, risking perforation, retained objects requiring urgent removal, burns, and airway obstruction.

    Product
    Single Use Distal Cover MAJ-2315 Used with: EVIS EXERA III Duodenovideoscope TJF-Q190V- designed to be attached to Olympus duodenovideoscopes to cover the distal end of the insertion tube and around the forceps elevator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1075-2024·2024-02-21

    Medical Device Control Panel Contaminated with Norovirus, Causes False Positive Results

    Microbiologics Enteric Pathogens Control Panel (Inactivated Pellet) negative control is contaminated with Norovirus. Users testing this control will incorrectly receive positive Norovirus results.

    Product
    Microbiologics Enteric Pathogens Control Panel (Inactivated Pellet), REF 8184.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1069-2024·2024-02-21

    Captus 4000e Thyroid Uptake Systems spring failure poses fall risk

    Mirion Technologies recalls 467 Captus 4000e Thyroid Uptake Systems due to spring arm failure that can cause the collimator to fall, posing potential injury risk to patients and operators.

    Product
    Captus 4000e Thyroid Uptake Systems- Intended to be used by trained Nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures. Models: 5430-30151, 5430-30152, and 5430-30154
    Category
    Medical Device
    Distribution
    Distributed nationwide