The Recall Desk

State

New York product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44426–44450 of 86773

  • HighNHTSA·18V524000·2018-08-09

    Chrysler, Jeep, and Ram Vehicles Recalled for Powertrain Control Module Defect

    FCA US LLC is recalling specific 2017-2019 Chrysler, Jeep, Ram, Dodge, and Fiat vehicles because a faulty voltage regulator chip may cause the vehicle to stall or fail to start.

    Product
    CHRYSLER — CHRYSLER, RAM, JEEP PACIFICA, PACIFICA PLUG-IN HYBRID, 1500, RENEGADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18202·2018-08-09

    Vitamix Recalls Ascent and Venturist Blending Containers Due to Laceration Hazard

    Vitamix is recalling Ascent and Venturist series blending containers because they can separate from the blade base, exposing blades and posing a laceration hazard.

    Product
    Ascent™ and Venturist™ Series 8-ounce and 20-ounce blending containers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V511000·2018-08-09

    Gillig Recalls Low Floor Buses Due to Turn Signal Flashing Defect

    Gillig is recalling 2012-2018 Low Floor buses because front and rear turn signals may flash at different rates, potentially confusing other drivers.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1675-2018·2018-08-08

    Probiotic Supplement Recalled for Potential Undeclared Allergens

    LL'S Magnetic Clay Inc. is recalling Prescript-Assist Probiotic & Prebiotic supplements because they may contain undeclared almonds, shellfish, milk, eggs, or peanuts.

    Product
    Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary Supplement, 60-capsule or 90-capsule bottles; UPC Codes: 853956003157, 853956003539
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2601-2018·2018-08-08

    Polysorb Suture Recalled for Potential Propylene Glycol Contamination

    Covidien LLC is recalling Polysorb Braided Absorbable Sutures due to potential propylene glycol contamination. The recall affects 972 units distributed in California, New York, and Texas.

    Product
    Polysorb Braided Absorbable Suture 1 36" 90 cm Undyed GS-21, Product Number CL-955
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Devices)·Z-2559-2018·2018-08-08

    Galt Medical Recalls Vascular Dilators and Introducer Kits Due to Endotoxins

    Galt Medical Corporation is recalling specific vascular dilators and introducer kits because they may contain unsafe levels of bacterial endotoxins introduced during manufacturing.

    Product
    1) Vascular Dilator, Sterile EO, Rx Only, Catalog #: DIL-100-12; 2) Dilator, Sterile EO, Rx Only, Catalog #: DIL-600-11; 3) Tearaway Introducer, Sterile EO, Rx Only, Catalog #: a) INT-028-14; b) INT-028-24; c) INT-029-05; d) INT-106-01; e) INT-106-14; 4) Micro-Access…
    Category
    Medical Device
    Distribution
    19 states
  • SevereFDA (Devices)·Z-2558-2018·2018-08-08

    Galt Medical Recalls Sterile Hemostasis Valve Introducer Systems Due to Endotoxins

    Galt Medical Corporation is recalling specific sterile hemostasis valve introducer systems and kits because they may contain unsafe levels of bacterial endotoxins introduced during manufacturing.

    Product
    1) ELITE HV, Hemostasis Valve Introducer System, Sterile EO, Rx Only, Catalog #: a) BCL-100-04; b) BCL-100-05; c) BCL-100-06; d) BCL-500-36; 2) Elite HV Introducer Set, Sterile EO, Rx Only, Catalog #: a) CLI-105-14; 3) AngioGate HV Introducer Kit, Sterile EO, Catalog #…
    Category
    Medical Device
    Distribution
    19 states
  • SevereFDA (Devices)·Z-2563-2018·2018-08-08

    Galt Medical Recalls Centeze Centesis Catheters Due to Bacterial Endotoxins

    Galt Medical Corporation is recalling 300 units of Centeze Centesis Catheters because they may contain unsafe levels of bacterial endotoxins introduced during manufacturing.

    Product
    Centeze Centesis Catheter, Catalog #: a) DRC-006-05, b) DRC-006-15,
    Category
    Medical Device
    Distribution
    19 states
  • SevereFDA (Drugs)·D-1023-2018·2018-08-08

    Pfizer Recalls Daptomycin Injection Due to Microbial Contamination

    Pfizer is recalling Daptomycin for Injection due to reports of adverse events indicative of infusion reactions related to microbiological contamination.

    Product
    Daptomycin for Injection, 500 mg per vial, packaged as 1 Single-dose vial per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-0106-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2594-2018·2018-08-08

    Integra LifeSciences Recalls Mayfield Infinity XR2 Base Units Due to Fracture Risk

    Integra LifeSciences is recalling Mayfield Infinity XR2 Low Profile Base Units because the knob assembly in the swivel adapter may fracture or break during use.

    Product
    MAYFIELD INFINITY XR2 LOW PROFILE BASE UNIT, Part Number A2079A The MAYFIELD¿ Infinity XR2 Base Unit is intended to be used to support a patient during diagnostic examination and/or surgical procedures where a rigid support between surgical table and headrest, or skull clamp…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2599-2018·2018-08-08

    Beckman Coulter MicroScan Pos Combo Panel Type 43 Recalled for Incorrect Moxifloxacin Dilution

    Beckman Coulter is recalling MicroScan Pos Combo Panel Type 43 because an incorrect Moxifloxacin dilution sequence may cause inaccurate antimicrobial susceptibility results.

    Product
    MicroScan Pos Combo Panel Type 43, Catalog number B1017-217for use in determining antimicrobial agent susceptibility and/or identification to the species level of rapidly growing aerobic and facultative gram-positive cocci, some fastidious aerobic gram-positive cocci and…
    Category
    Medical Device
    Distribution
    12 states
  • HighFDA (Food)·F-1810-2018·2018-08-08

    Innova Flavors Recalls Natural Butter Flavor Due to Salmonella Risk

    Innova Flavors is voluntarily recalling specific lots of Natural Butter Flavor because a supplier's sweet whey powder ingredient is potentially contaminated with Salmonella.

    Product
    Natural Butter Flavor, 40 pounds, Powder in a blue poly-lined cardboard box, Ambient
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1894-2018·2018-08-08

    Griffith Labs Herb Crouton Seasoning Recalled for Potential Salmonella

    Griffith Labs U.S.A. is recalling 50-pound bags of Herb Crouton Seasoning due to the potential presence of Salmonella from a recalled whey ingredient.

    Product
    Herb Crouton Seasoning 50 pound bag Item 702046300
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2562-2018·2018-08-08

    Galt Medical Elite HV Introducer Recalled for Bacterial Endotoxins

    Galt Medical Corporation is recalling Elite HV Introducers due to potential unsafe levels of bacterial endotoxins introduced during manufacturing.

    Product
    Elite HV Introducer, Catalog #: a) CLI-200-26; b) CLI-210-16; c) CLI-212-07; d) KCL-212-055
    Category
    Medical Device
    Distribution
    19 states
  • HighFDA (Devices)·Z-2602-2018·2018-08-08

    Zimmer Dermatone AN Skin Graft Device Recalled for Loose Control Bar

    Zimmer Surgical Inc is recalling 140 units of the Zimmer Dermatone AN skin graft device due to a loose control bar that may compromise graft thickness control.

    Product
    Zimmer Dermatone AN, Model No. 88710100
    Category
    Medical Device
    Distribution
    17 states
  • HighFDA (Food)·F-1864-2018·2018-08-08

    Griffith Labs Recalls Low Sodium Brown Gravy Mix for Salmonella Risk

    Griffith Labs U.S.A. is recalling Low Sodium Brown Gravy Mix due to the potential presence of Salmonella from a recalled whey ingredient.

    Product
    Low Sodium Brown Gravy Mix 12 oz unit, 8 units per carton Item 860143100 UPC 9624817431
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1869-2018·2018-08-08

    Griffith Labs Recalls Reduced Whey Cold Dough Premix Due to Salmonella Risk

    Griffith Labs U.S.A. is recalling Reduced Whey Cold Dough Premix because it may contain Salmonella from a recalled whey ingredient. The product was distributed nationwide and in Canada.

    Product
    Reduced Whey Cold Dough Premix 2.3 pound bag, 18 units per carton Item 127038500
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1858-2018·2018-08-08

    Griffith Labs Recalls Biscuit Mix Due to Potential Salmonella Risk

    Griffith Labs U.S.A. is recalling specific lots of Biscuit Mix because it may contain Salmonella from a recalled whey ingredient.

    Product
    Biscuit Mix 4.5 pound bag, 8 bags per carton Item 127042301
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1863-2018·2018-08-08

    Griffith Labs Recalls Beef Flavored Gravy Mix Due to Salmonella Risk

    Griffith Labs U.S.A. is recalling Beef Flavored Gravy Mix because it may contain Salmonella from a recalled whey ingredient.

    Product
    Beef Flavored Gravy Mix 12 oz unit, 8 units per carton Item 860143801 UPC 9624817621
    Category
    Food
    Distribution
    Distributed nationwide