The Recall Desk

State

New York product recalls

73,741 recalls have nationwide distribution and so reach New York. 12,955 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total
12,955
Critical
1,508
Severe
3,701
Most recent
2026-10-28

Of the 12,955 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 3,701 (29%) are Severe.

Which agencies issued them

These figures cover only the 12,955 recalls whose distribution notice names New York specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35726–35750 of 86696

  • HighFDA (Devices)·Z-0803-2020·2020-01-22

    Flexicare BriteBlade Pro Laryngoscope Blades Recalled for Loose Components

    Flexicare Medical Ltd. is recalling BriteBlade Pro laryngoscope blades because internal spring, washer, and bearing components may become loose and separate from the device.

    Product
    BriteBlade Pro Single-Use Fiber Optic Handle and Blade Mac 3, CE 0120, Do not Re-use, Rx Only, REF, 040-333U, Sterile EO, Qty 10, (01)15055788724138(17)230801(10)180900072 The device is intended for direct vision laryngoscopy to obtain an illuminated view of the vocal cords…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0552-2020·2020-01-22

    Wegmans Recalls Lobster Stuffed Tilapia for Undeclared Soy

    Wegmans is recalling Lobster Stuffed Tilapia because the product contains undeclared soy. Consumers with soy allergies should not eat the product.

    Product
    Lobster Stuffed Tilapia; Wegmans Ready to Cook Lobster Stuffed Tilapia, 7 oz; Unit size 7oz; Oven Ready Tray; Package size 7oz; Keep Refrigerated or Frozen
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0542-2020·2020-01-22

    Wegmans Recalls Salmon with Crab Stuffing Due to Undeclared Soy

    Wegmans is recalling Salmon with Crab Stuffing because the product contains undeclared soy. Consumers should not eat the product and should return it to the store.

    Product
    Salmon with Crab Stuffing; Wegmans Salmon Topped with Crab Stuffing; 8 oz; Oven ready tray; Keep Refrigerated or Frozen
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0550-2020·2020-01-22

    Wegmans Recalls Lobster Stuffed Mushrooms for Undeclared Soy

    Wegmans is recalling Lobster Stuffed Mushrooms because they contain undeclared soy. The product was sold in seven states.

    Product
    Lobster Stuffed Mushrooms; Wegmans Ready to Cook Lobster Stuffed Mushrooms, Sold by the lb; Unit size varies; Oven ready tray; Package size varies; Keep Refrigerated or Frozen
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0816-2020·2020-01-22

    Physio-Control Recalls LIFEPAK 15 Monitor/Defibrillators Due to Keypad Oxidation

    Physio-Control is recalling 29,952 LIFEPAK 15 Monitor/Defibrillators worldwide because oxidation on the keypad may prevent the device from delivering a shock.

    Product
    LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an affected keypad.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0547-2020·2020-01-22

    Wegmans Lobster Stuffed Salmon Recalled for Undeclared Soy

    Wegmans is recalling Lobster Stuffed Salmon products because they contain undeclared soy. Consumers with soy allergies should not eat the product.

    Product
    Lobster Stuffed Salmon; Wegmans Ready to Cook Salmon Topped with Loster, 7 oz; oven ready tray; Keep Refrigerated or Frozen
    Category
    Food
    Distribution
    7 states
  • HighFDA (Drugs)·D-0773-2020·2020-01-22

    Assurance Infusion Recalls TRIMIX Injection Vials Due to Sterility Concerns

    Assurance Infusion is recalling 1,290 vials of TRIMIX injection nationwide due to a lack of sterility assurance. No specific illnesses or injuries are reported in the source text.

    Product
    TRIMIX 30MG/1MG/10MCG/ML INJ in 5 mL/10 mL vials Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0534-2020·2020-01-22

    Wegmans Recalls Crab Stuffed Salmon for Undeclared Soy Allergen

    Wegmans is recalling Crab Stuffed Salmon products because they contain undeclared soy. Consumers with soy allergies should not eat these items.

    Product
    Crab Stuffed Salmon; Crab Stuffed Salmon with Lemon Tarragon sauce; 1 each; Oven ready tray; Varied sizes; Keep Refrigerated
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Food)·F-0522-2020·2020-01-22

    Bob's Red Mills Recalls Garbanzo Beans for Potential Glyphosate

    Bob's Red Mills is recalling specific 25 oz packages of Garbanzo Beans due to the potential presence of glyphosate. The recall affects products distributed in the US and several international locations.

    Product
    Garbanzo Beans or Chickpeas, sold under brand Bob's Red Mills, packaged into 25 oz Form & Fill Package or 25 oz Standup Package. 25 oz Form & Fill Package Package has UPC 039978004222. 25 oz Standup Package has UPC 039978114228
    Category
    Food
    Distribution
    13 states
  • ModerateFDA (Drugs)·D-0802-2020·2020-01-22

    McGuff Compounding Pharmacy Recalls Lipoic Acid Injection Due to Particulate Matter

    McGuff Compounding Pharmacy Services is recalling Lipoic Acid Injection vials because filmy or cloudy particulate matter was observed in the product.

    Product
    Lipoic Acid Injection (aka Alpha Lipoic Acid or Thioctic Acid), 1,200 mg/30 mL (40 mg/mL) Sterile 30 mL Multiple Dose Vial, Rx Only, McGuff Compounding Pharmacy Services, Inc., Santa Ana, CA 92704
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0812-2020·2020-01-22

    Microbiologics Gram-Positive Blood Culture Control Panel Recall for Hydration Fluid Change

    Microbiologics Inc is recalling 810 units of the Gram-Positive Blood Culture Control Panel because the recommended hydration fluid has changed to sterile DI water or pH 7.2 phosphate buffer.

    Product
    Microbiologics QC Sets and Panels, Gram-Positive Blood Culture Control Panel (Inactivated Pellet), Catalog # 8180 Used in test systems to estimate test precision and to detect systematic analytical deviations that may arise from reagent or analytical instrument variation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0805-2020·2020-01-22

    Caire FreeStyle Comfort Oxygen Concentrators Recalled for Lack of US Clearance

    Caire, Inc. is recalling four European version FreeStyle Comfort Oxygen Concentrators because they were not cleared for use in the US.

    Product
    CAIRE MODEL: FreeStyle Comfort Oxygen Concentrator - Product Usage: The FreeStyle Comfort Oxygen Concentrator is intended for the administration of supplemental oxygen. The device is not intended for life support nor does it provide any patient monitoring capabilities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0521-2020·2020-01-22

    Bob's Red Mill 13 Bean Soup Mix Recalled for Glyphosate

    Bob's Red Mill is recalling 13 Bean Soup Mix due to the potential presence of glyphosate. The product was distributed in multiple US states and international locations.

    Product
    13 Bean Soup Mix is sold under Bob's Red Mill brand, packaged in Form & Fill (29 oz. and 822 gram), Standup Pouch (29 oz.), and Bulk Bags (25 lbs.) Product has the following UPC: UPC: 039978122513 UPC: 039978002518 UPC: 039978102515 (25 lb. bag) UPC: 039978302519…
    Category
    Food
    Distribution
    13 states
  • LowFDA (Drugs)·D-0789-2020·2020-01-22

    AuroMedics Recalls Moxifloxacin Ophthalmic Solution Due to Discoloration

    AuroMedics Pharma LLC is recalling Moxifloxacin Ophthalmic Solution due to market complaints of discoloration. The affected product is distributed nationwide in the U.S.

    Product
    MOXIFLOXACIN — MOXIFLOXACIN (MOXIFLOXACIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0790-2020·2020-01-22

    Lupin Recalls Tri-Lo-Marzia Tablets Due to Blend Uniformity Deviations

    Lupin Pharmaceuticals is recalling specific lots of Tri-Lo-Marzia oral contraceptives due to out-of-specification test results found during a retrospective review of blend uniformity data.

    Product
    Tri-Lo-Marzia (Norgestimate and Ethinyl Estradiol Tablets, USP), 0.180 mg/0.025 mg; 0.215mg/0.025 mg and 0.250 mg/0.025 mg, Pack size - 3 x 28's wallets/carton, Rx Only, Distributed by Lupin Pharmaceuticals, Inc, Baltimore MD 21202, Manufactured by: Lupin Limited, Pithampur…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V032000·2020-01-20

    Arcimoto Recalls 2019 FUV Motorcycles Due to Brake Line Wear Risk

    Arcimoto is recalling 2019 FUV motorcycles because the brake line may contact the steering main-link, potentially causing a loss of braking ability and increasing crash risk.

    Product
    ARCIMOTO — ARCIMOTO FUV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V023000·2020-01-17

    Terex Advance Mixer Recalls 2020 Concrete Mixers Due to Axle Shaft Fracture Risk

    Terex Advance Mixer is recalling 2020 FDC300, FD4000, FD5000GL, and FD7000B vehicles because incorrectly heat-treated axle output shafts may fracture, causing loss of drive and increasing crash risk.

    Product
    TEREX ADVANCE — TEREX ADVANCE FDC300, FD5000GL, FD4000, FD7000B
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V024000·2020-01-17

    Toyota Recalls Corolla, Matrix, Avalon Models for Air Bag Defect

    Toyota is recalling specific 2011-2019 Corolla, Matrix, Avalon, and Avalon Hybrid vehicles because the air bag control unit may malfunction, potentially preventing air bags and seat belt pretensioners from deploying in a crash.

    Product
    TOYOTA — TOYOTA AVALON, AVALON HYBRID, MATRIX, COROLLA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V026000·2020-01-17

    Honda, Acura, and Isuzu Recall Vehicles for Air Bag Inflator Defect

    Honda is recalling specific Acura, Honda, and Isuzu vehicles because driver air bag inflators may rupture or underinflate, posing a risk of injury.

    Product
    ISUZU — ISUZU, HONDA, ACURA OASIS, CIVIC, CR-V, EV PLUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V027000·2020-01-17

    Honda Recalls Vehicles for Driver Air Bag Inflator Rupture Risk

    Honda is recalling specific 2000-2003 Acura and Honda vehicles because replacement driver air bag inflators may rupture or underinflate in a crash, increasing injury risk.

    Product
    ACURA — ACURA, HONDA MDX, CL, ODYSSEY, RL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V022000·2020-01-17

    Hyundai Recalls 2020 Kona Vehicles for Incorrect Weight Rating Label

    Hyundai is recalling 2020 Kona vehicles because the certification label may display an incorrect Gross Axle Weight Rating. Dealers will replace the label to ensure compliance with federal safety standards.

    Product
    HYUNDAI — HYUNDAI KONA
    Category
    Vehicle
    Distribution
    Distributed nationwide