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.

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.

37726–37750 of 86696

  • HighFDA (Food)·F-2121-2019·2019-09-18

    Martha White Gluten Free Cornbread Mix Recalled for Gluten Presence

    Hometown Food Company is recalling Martha White Gluten Free Sweet Yellow Cornbread & Muffin Mix because the product tested positive for gluten despite being labeled gluten-free.

    Product
    Martha White Gluten Free Sweet Yellow Cornbread & Muffin Mix packaged in a 7oz. pouch. 12 pouches per wholesale case. Item UPC: 0 1330082014 8.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2499-2019·2019-09-18

    Exactech Recalls Threaded Offset Cup Impactor Due to Gritty Mechanism

    Exactech, Inc. is recalling 22 Threaded Offset Cup Impactors because the threaded mechanism may be gritty and difficult to turn, potentially due to entrapped blast media.

    Product
    Threaded Offset Cup Impactor - Product Usage: To assist the surgeon in the implantation of Novation hip system components according to a conventional technique for total hip replacement. Specifically, these instruments are reusable, surgically invasive, and intended for…
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Drugs)·D-1851-2019·2019-09-18

    Macleods Recalls Pramipexole Dihydrochloride Tablets Due to Subpotency

    Macleods Pharma USA is recalling Pramipexole Dihydrochloride Tablets 0.125 mg because stability studies showed the drug was subpotent.

    Product
    PRAMIPEXOLE DIHYDROCHLORIDE — PRAMIPEXOLE DIHYDROCHLORIDE (PRAMIPEXOLE DIHYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2495-2019·2019-09-18

    Philips 5-Lead ECG Set Recalled Due to Connector Thickness Issue

    Philips is recalling 5-Lead ECG sets because the connector thickness may prevent or impede I 2-Lead ECG measurements.

    Product
    Philips 5-Lead Set, Disposable, Bedside, AAMI Model # 989803173131 Product Usage: Philips Single-Patient-Use ECG lead sets for bedside monitoring are available in 5-lead configuration
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2151-2019·2019-09-18

    FungusAmongUs Shiitake Organic Mushrooms Recalled for Undeclared Sulfites

    Seattle Gourmet Foods Inc. is recalling FungusAmongUs Shiitake Organic Mushrooms due to undeclared sulfites detected by the Florida Department of Agriculture.

    Product
    FungusAmongUs Shiitake Organic Mushrooms are dried mushrooms. Packaged in a clear cellophane bag, net Weight 1 ounce. UPC 7 19870 60023 3 for individual 1 ounce bags UPC 50719870600016 for Master caddy that holds 8 packages of 1 ounce bags The label is read in parts…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2488-2019·2019-09-18

    Philips Recalls Two HeartStart MRx Monitor/Defibrillators for Missing Corrections

    Philips North America, LLC is recalling two HeartStart MRx Monitor/Defibrillators because they may not have received applicable corrections from prior field actions.

    Product
    HeartStart MRx Monitor/Defibrillator Model # M3535A - Product Usage: The HeartStart MRx is a lightweight, portable external defibrillator, offering two modes of operation for defibrillation: manual mode and semi-automatic mode (AED). In manual mode, the HeartStart MRx is a full…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2153-2019·2019-09-18

    Abbott Recalls Similac Pro-Sensitive Bottles Due to Packaging Error

    Abbott Nutrition is recalling specific cartons of Similac Pro-Sensitive that may contain Similac Pro-Advance bottles due to a packaging error.

    Product
    Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton.
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Food)·F-2144-2019·2019-09-18

    Calcium Supplement Recalled for Lacking Declared Vitamin D Content

    Jivan Shakti Inc. is recalling 790 bottles of Dr. Naram's Rasayana D Tablet because FDA testing found no Vitamin D in the product.

    Product
    Plastic Bottles labeled with: "Ancient Youth Secret - Since 500 B.C., DR. NARAM'S RASAYANA D TABLET, Calcium Supplement with Vitamin D*, Dietary Supplement, 60 Tablets, FOR EXPORT ONLY, Imported & Distributed by: Jivan Shakti INC, 933 South Street, Peekskill, NY 10566…
    Category
    Food
    Distribution
    20 states
  • ModerateFDA (Food)·F-2152-2019·2019-09-18

    Stonyfield Kids Strawberry Beet Berry Tubes Recalled for Misbranding

    Stonyfield Farm is recalling 4,064 cartons of Kids Strawberry Beet Berry Tubes because the outer carton labeling does not match the product.

    Product
    Stonyfield Kids Strawberry Beet Berry Tubes, 8 count-2oz each; 453g/package; Keep Refrigerated
    Category
    Food
    Distribution
    6 states
  • LowFDA (Drugs)·D-1848-2019·2019-09-18

    Mylan Recalls Gatifloxacin Ophthalmic Solution Due to Unknown Impurity

    Mylan Pharmaceuticals is recalling Gatifloxacin Ophthalmic Solution 0.5% due to an out-of-specification result for an unknown impurity.

    Product
    Gatifloxacin Ophthalmic Solution 0.5%, 2.5 mL per bottle, Rx Only, Mfd. for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505. Made in India. NDC: 0378-5431-35
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2490-2019·2019-09-18

    Randox Calibration Serum Recalled for Incorrect Analyte Targets

    Randox Laboratories is recalling calibration sera due to realigned targets for AST and ALT. The recall affects 307 kits distributed nationwide and in several foreign locations.

    Product
    This is an in vitro diagnostic product intended for use as a calibration serum in clinical chemistry assays. Randox calibration sera contain 42 analytes and are based on lyophilized human serum. The concentrations and activities are suitable for calibration of clinical chemistry…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1847-2019·2019-09-18

    Lamivudine Tablets Recalled for Incorrect Package Insert Labeling

    American Health Packaging is recalling Lamivudine Tablets due to an error in the package insert that incorrectly lists tablet description coding.

    Product
    Lamivudine Tablets, USP, 150 mg, 30 (3x10) count Unit Dose Blisters Carton, NDC 60687-362-21 (Individual Dose NDC: 60687-362-11), Distributed by American Health Packaging, Columbus, OH
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V656000·2019-09-17

    McNeilus CNG Trucks Recalled for Pressure Relief Device Defect

    McNeilus is recalling 330 CNG-powered trucks from 2013-2018 because pressure relief devices may fail to vent pressure, increasing the risk of tank explosion, fire, and injury.

    Product
    MCNEILUS — MCNEILUS AUTOREACH, STANDARD MIXER, ZERO RADIUS, ATLANTIC FRONT LOADER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V658000·2019-09-17

    Hyundai Translead Recalls 2017-2018 Duralite HT Flatbed Trailers

    Hyundai Translead is recalling 2017-2018 Duralite HT flatbed trailers because bulkhead brackets may break, causing the bulkhead to detach and create a road hazard.

    Product
    HYUNDAI TRANSLEAD — HYUNDAI TRANSLEAD DURALITE HT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V659000·2019-09-17

    Terex TLM Aerial Vehicles Recalled for Boom Valve Defect

    Terex is recalling 2016-2017 TLM aerial devices because an incorrect holding valve may cause the boom to drift down if a hose bursts.

    Product
    TEREX — TEREX TLM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V655000·2019-09-16

    Airstream Recalls 2016-2017 Trailers Due to Electrical Fire Risk

    Airstream is recalling specific 2016-2017 Flying Cloud and International trailers because an inverter may contact a fuse, creating a fire hazard.

    Product
    AIRSTREAM — AIRSTREAM FLYING CLOUD, INTERNATIONAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V654000·2019-09-12

    Nissan and Infiniti Recall Vehicles for Backup Camera Display Defect

    Nissan is recalling 2018-2019 Nissan and Infiniti vehicles because backup camera settings can be adjusted to hide the rear view image, increasing crash risk.

    Product
    NISSAN — NISSAN, INFINITI ROGUE SPORT, ARMADA, VERSA, ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E062000·2019-09-12

    Chrysler Recalls Mopar Passenger Air Bag Modules Due to Testing Defect

    Chrysler is recalling specific Mopar replacement passenger air bag modules that did not complete developmental testing. These modules may not perform as designed in a crash, increasing injury risk.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide