The Recall Desk

State

New York product recalls

73,809 recalls have nationwide distribution and so reach New York. 12,956 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total
12,956
Critical
1,508
Severe
3,702
Most recent
2026-11-04

Of the 12,956 recalls naming New York we have scored against our rubric, 1,508 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,702 (29%) are Severe.

These figures cover only the 12,956 recalls whose distribution notice names New York specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42101–42125 of 86765

  • ModerateFDA (Devices)·Z-0660-2019·2019-01-02

    Randox SP CAL (LIQ) Calibrator Recall for Value Sheet Corrections

    Randox Laboratories is recalling SP CAL (LIQ) calibrators because value sheets were modified to improve alignment for specific assays.

    Product
    SP CAL (LIQ), REF IT2692 This product is intended for in vitro diagnostic use with Randox Alpha-1-Antitrypsin, Alpha-1-Acid Glycoprotein, IgA, IgG and IgM assays that require sample predilution.
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-0685-2019·2019-01-02

    Hologic I-View Contrast Enhanced Digital Mammography System Recall

    Hologic is recalling 337 I-View Contrast Enhanced Digital Mammography systems due to a calibration issue that prevents visualization of contrast uptake.

    Product
    I-View¿ Contrast Enhanced Digital Mammography, ASY-08109
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0676-2019·2019-01-02

    Tosoh Bioscience Recalls ST AIA-PACK ACTH In Vitro Diagnostic Reagents

    Tosoh Bioscience Inc is voluntarily recalling 1,085 units of ST AIA-PACK ACTH in vitro diagnostic reagents distributed nationwide in the US.

    Product
    ST AIA-PACK ACTH (ACTH: Adrenocorticotropic Hormone) is designed for IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of Adrenocorticotropic hormone (ACTH) in human EDT A plasma. Measurements of ACTH are used in the differential diagnosis and treatment of certain…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0671-2019·2019-01-02

    Tosoh AIA-PACK B12 Recalled Due to Potential Fluorescein Interference

    Tosoh Bioscience Inc is recalling AIA-PACK B12 reagents because fluorescein interference may cause inaccurately elevated Vitamin B12 test results.

    Product
    AIA-PACK B12 (Vitamin B12) is designed for IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of vitamin B12 (B12) in human serum on Tosoh AIA System analyzers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0675-2019·2019-01-02

    Tosoh Bioscience Recalls ST AIA-PACK Homocysteine Diagnostic Reagents

    Tosoh Bioscience is recalling 992 units of ST AIA-PACK Homocysteine reagents used for in vitro diagnostic testing. The voluntary recall covers all lots distributed nationwide.

    Product
    ST AIA-PACK Homocysteine (HCY) is designed for IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of homocysteine in human serum, heparinized plasma or EDT A plasma on TOSOH AIA System Analyzers. Homocysteine measurements are used in the diagnosis and treatment of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V944000·2018-12-31

    Arcimoto Recalls 2018 FUV Motorcycles Due to Transmission Defect

    Arcimoto is recalling 2018 FUV motorcycles because incorrect machining of the transmission case may cause premature gearbox failure, potentially immobilizing the vehicle and increasing crash risk.

    Product
    ARCIMOTO — ARCIMOTO FUV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V937000·2018-12-31

    Arcimoto Recalls 2017 FUV Motorcycles Due to Brake System Defect

    Arcimoto is recalling 2017 FUV motorcycles because the brake system design may fail to meet federal stopping distance requirements, increasing crash risk.

    Product
    ARCIMOTO — ARCIMOTO FUV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V940000·2018-12-31

    Arcimoto Recalls 2017 FUV Motorcycles Due to Brake Fitting Defect

    Arcimoto is recalling 2017 FUV motorcycles because incorrect fittings in the braking system may cause fluid leaks, reducing brake effectiveness and increasing crash risk.

    Product
    ARCIMOTO — ARCIMOTO FUV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V943000·2018-12-31

    Arcimoto Recalls 2017-2018 FUV Motorcycles for Headlight Spacing Defect

    Arcimoto is recalling 2017-2018 FUV motorcycles because the headlights may be spaced too far apart, making the vehicle difficult to recognize as a motorcycle in the dark.

    Product
    ARCIMOTO — ARCIMOTO FUV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V942000·2018-12-31

    Arcimoto Recalls 2017-2018 FUV Motorcycles for Missing Side Reflectors

    Arcimoto is recalling 2017-2018 FUV motorcycles because the rear light assembly lacks required side reflex reflectors, reducing visibility and increasing crash risk.

    Product
    ARCIMOTO — ARCIMOTO FUV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V941000·2018-12-31

    Arcimoto Recalls 2017-2018 FUV Motorcycles for Turn Signal Placement

    Arcimoto is recalling 2017-2018 FUV motorcycles because front turn signals are not positioned as required by federal safety standards, potentially reducing visibility.

    Product
    ARCIMOTO — ARCIMOTO FUV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V935000·2018-12-31

    Subaru Recalls 2018 Models for Rearview Camera Software Defect

    Subaru is recalling 2018 Legacy, Outback, and BRZ vehicles because a software issue may prevent the rearview camera from displaying an image while backing up.

    Product
    SUBARU — SUBARU OUTBACK, LEGACY, BRZ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·125-2018·2018-12-30

    Zeigler Red Hot Sausage Recalled for Metal Contamination

    R. L. Zeigler Co. is recalling Red Hot chicken and pork sausage products due to possible metal contamination. No illnesses have been reported.

    Product
    R. L. Zeigler Co. Inc. — R. L. Zeigler Co., Inc. Recalls Chicken and Pork Red Hot Sausage Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V934000·2018-12-28

    Hyundai Recalls Sonata and Santa Fe Sport for Fuel Pipe Fire Risk

    Hyundai is recalling 2011-2014 Sonata and 2013-2014 Santa Fe Sport vehicles because a fuel pipe may leak, increasing the risk of a fire.

    Product
    HYUNDAI — HYUNDAI SONATA, SANTA FE SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V933000·2018-12-27

    Forest River Recalls 2019 Salem and Wildwood Trailers for Fire Risk

    Forest River is recalling 2019 Salem and Wildwood recreational trailers because the power cord hatch is located above the water heater exhaust, which may cause melting and increase fire risk.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0730-2019·2018-12-26

    Achdut Recalls Tahini Products Due to Potential Salmonella Contamination

    Achdut is recalling specific Baron's and Galil tahini products because they may be contaminated with Salmonella. The products were distributed in New York, California, Pennsylvania, and Israel.

    Product
    Tahini sold under the following brand names: Baron's Tahini double pack, 454g, UPC: X000EZ2HCB; Galil whole tahini, 500g, UPC: 814968020037
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0775-2019·2018-12-26

    Inspired Organic Sunflower Butter Recalled for Listeria monocytogenes Contamination

    Lipari Foods is recalling Inspired Organic Sunflower Butter because product testing found Listeria monocytogenes. The recall covers 972 cases distributed across 15 states and Canada.

    Product
    Inspired Organic Sunflower Butter 16oz. plastic jar, 6 per case UPC #: 863669742526 refrigerate after opening
    Category
    Food
    Distribution
    15 states