The Recall Desk

State

New York product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53151–53175 of 86789

  • SevereFDA (Food)·F-1209-2017·2017-01-18

    All American Seasonings Recalls Spicy Nacho Seasoning Due to Salmonella Risk

    All American Seasonings, Inc. is recalling 211 bags of 50 lb Spicy Nacho seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canadian consignees.

    Product
    Spicy Nacho. Product Code: T3552. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0964-2017·2017-01-18

    Stryker Recalls Reprocessed Electrophysiology Catheter Cables Due to Sterility Breach

    Stryker Sustainability Solutions is recalling reprocessed electrophysiology catheter cables because a breach in sterile packaging may have occurred, potentially rendering the product non-sterile.

    Product
    Reprocessed Electrophysiology Catheter Cables Catalog Number: CB3434CT, D134401, CB3410CT, CB3412CT Electrophysiology catheter cables are designed as electrode cables with a multi-pin connector on the distal end and the appropriate number of tails on the proximal end. The…
    Category
    Medical Device
    Distribution
    35 states
  • HighFDA (Devices)·Z-0987-2017·2017-01-18

    Elekta Oncentra Radiation Therapy Software Recalled for Cross Profile Defect

    Elekta, Inc. is recalling Oncentra External Beam and Brachy software because a cross profile for a Varian 60-degree wedge shows 'horns.' The recall covers 433 units distributed worldwide.

    Product
    Oncentra External Beam Oncentra Brachy Product Usage: Oncentra is radiation therapy planning software designed to analyze and plan radiation treatment is three dimensions for the purpose of treating patients with cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1218-2017·2017-01-18

    Stonewall Kitchen Orange Cranberry Pancake Mix Recalled for Salmonella Risk

    Stonewall Kitchen is recalling 40 units of Orange Cranberry Pancake & Waffle Mix due to potential salmonella contamination. The product was distributed in six states.

    Product
    Stonewall Kitchen Orange Cranberry Pancake & Waffle Mix, Packaged in a 16oz. canister UPC: 711381325971 Item #: 554130
    Category
    Food
    Distribution
    6 states
  • HighFDA (Drugs)·D-0430-2017·2017-01-18

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because the delivery system failed to meet mechanical peel force specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0877-2017·2017-01-18

    Capitol City Specialties Recalls Peanut Butter Jars for Undeclared Soy Lecithin

    Capitol City Specialties Company is recalling 900 jars of Dashing Thru the Dough Gourmet Chocolate Chip Cookie Dough Peanut Butter due to undeclared soy lecithin.

    Product
    the Peanut Principle, Dashing Thru the Dough, Gourmet Chocolate Chip Cookie Dough Peanut Butter, NET WT 16oz, UPC 609207898788
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1252-2017·2017-01-18

    Roy Roger's Pancake Mix Recalled for Possible Salmonella Contamination

    House-Autry Mills is recalling Roy Roger's Pancake Mix because it contains milk product from a supplier recalling for possible Salmonella.

    Product
    Roy Roger's Pancake Mix, Net Wt., 2 lb. 8 oz. bags, UPC Code 0 73484 22724 0
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0967-2017·2017-01-18

    C.R. Bard Recalls Medical Devices Containing Latex Catheters

    C.R. Bard is recalling specific medical device trays and stabilization devices because they contained latex catheters instead of silicone catheters.

    Product
    SURESTEP Tray, BARDEX I.C. COMPLETE CARE, Urine Meter, Temperature STATLOCK Stabilization Device
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-1006-2017·2017-01-18

    Philips IQon Spectral CT Recalled for Image and Scan Errors

    Philips is recalling 35 IQon Spectral CT systems due to software issues causing rescans, incorrect scan locations, or misrepresentation of image results.

    Product
    IQon Spectral CT with software version 4.7.0 Product Usage: The IQon Spectral CT is a Computed Tomography X-Ray System intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes. This…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1225-2017·2017-01-18

    Brand Castle Monkey Bread Mix Recalled for Salmonella

    Brand Castle LLC is recalling In The Mix Monkey Bread Mix because the facility and finished product tested positive for Salmonella.

    Product
    In The Mix¿ Monkey Bread Mix NET WT 16 oz (16 lb) 454 g box, INGREDIENTS: BREAD MIX: ***BUTTERMILK*** DISTRIBUTED BY BRAND CASTLE, LLC BEDFORD HTS, OH 44146 www.brandcastle.com UPC 8 44527 03278 2
    Category
    Food
    Distribution
    38 states
  • HighFDA (Food)·F-1217-2017·2017-01-18

    Stonewall Kitchen Cinnamon Apple Pancake Mix Recalled for Salmonella Risk

    Stonewall Kitchen is recalling Cinnamon Apple Pancake & Waffle Mix due to potential Salmonella contamination. Consumers should stop using the product.

    Product
    Stonewall Kitchen Cinnamon Apple Pancake & Waffle Mix, 16 oz. canister UPC: 711381025659 Item #: 551118
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-1247-2017·2017-01-18

    House-Autry Buttermilk Biscuit Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling Buttermilk Biscuit Mix because it contains milk from a supplier recalling product due to possible Salmonella.

    Product
    House-Autry Buttermilk Biscuit Mix Tote, Net Wt., 8 oz. (227 g.), UPC Code 0 73484 15500 9,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-1007-2017·2017-01-18

    Medtronic Recalls AxIEM Touch N Go Pointer Probe for Accuracy Issues

    Medtronic Navigation is voluntarily recalling 111 AxIEM Touch N Go Pointer Probes because they may compromise navigation accuracy during patient registration.

    Product
    AxIEM Touch N Go Pointer Probe. Model Number: 9735318. Placed in a 30mil PETG tray sealed with a Tyvek lid and then placed in a shelf carton.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1249-2017·2017-01-18

    House-Autry Butterflake Biscuit Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling 606 bags of Butterflake Biscuit Mix because it contains milk product from a supplier recalling for possible Salmonella.

    Product
    House-Autry Butterflake Biscuit Mix, Net Wt. 25 lb. bags, UPC Code 0 73484 20513 1,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1250-2017·2017-01-18

    Buddy's Bar-B-Q Hushpuppy Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling Buddy's Bar-B-Q Hushpuppy Mix because it contains milk product from a supplier recalling for possible Salmonella.

    Product
    Buddy's Bar-B-Q Hushpuppy Mix, Net Wt., 5 lb bags, UPC Code 0 73484 22156 2,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0972-2017·2017-01-18

    Siemens Recalls Artis Q Angiographic X-Ray Systems for Generator Defects

    Siemens is recalling Artis Q angiographic x-ray systems due to potential high-voltage generator failures and rare image display loss.

    Product
    Artis Q/Q.zen, Angiographic x-ray system Stand alone system The Artis systems are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0988-2017·2017-01-18

    ICU Medical Recalls Tego Connectors Due to Potential Leaking Risk

    ICU Medical is recalling Tego Connectors due to a potential risk of leaking. The devices are used as accessories for vascular access in hemodialysis.

    Product
    Tego Connector, Item No. D1000, NM1000 The Tego¿ Needle Free Access Device is intended for use as an accessory to a vascular access device (catheter) used in Hemodialysis or as an accessory to an Intravascular Administration Set for the administration or withdrawal of fluids…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1224-2017·2017-01-18

    New Hope Mills Recalls Crepe Mix Due to Salmonella Risk

    New Hope Mills is recalling specific lots of Crepe Mix because the bulk milk powder used may be contaminated with Salmonella.

    Product
    NEW HOPE MILLS Crepe MIX, NET WT. 1 LB. 4 OZ, UPC 074703601529 --- 181 York Street, Auburn, New York 13021 ---Product is packaged in a brown paper bag
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0963-2017·2017-01-18

    Stryker Recalls Reprocessed Ablation Catheter Cables Due to Sterility Concerns

    Stryker is recalling reprocessed ablation catheter cables because a breach in sterile packaging may have resulted in non-sterile product.

    Product
    Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT, CR3434CT Ablation catheter cables are designed as electrode cables with a multi-pin connector on the distal end which connects to an ablation catheter and a multi-pin connector on the proximal end which connects…
    Category
    Medical Device
    Distribution
    35 states
  • HighFDA (Food)·F-1248-2017·2017-01-18

    House-Autry Cheese Biscuit Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling Cheese Biscuit Mix because it contains milk from a supplier recalling product for possible Salmonella.

    Product
    House-Autry Cheese Biscuit Mix, Net Wt., 8 oz. (227 g.), UPC Code 0 73484 15510 8,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-1005-2017·2017-01-18

    Philips Clinix RF Plus X-ray System Recalled for Tilt Hazard

    Philips is recalling 41 Clinix RF Plus X-ray systems because liquid penetration can cause an unintentional tilt of the diagnostic table.

    Product
    FV-RF (Clinix RF Plus) Product Usage: A Stationary X-ray System, a device intended for radiographic/fluoroscopic examinations of various anatomical regions. This device may include signal analysis and display equipment, patient and equipment supports, components and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V040000·2017-01-18

    Nissan Recalls 2015-2017 Altima Vehicles for Rear Door Latch Defect

    Nissan is recalling 2015-2017 Altima vehicles because improperly routed rear door latch cables may allow doors to open while driving, increasing injury risk.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide